Linked Data
dbSNP Id:
rs777613969
ExAC:
12:103271232 G / C
gnomAD v2:
12-103271232-G-C
gnomAD v4:
12-102877454-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102877454G>C , CM000674.2:g.102877454G>C | GRCh38 |
| NC_000012.11:g.103271232G>C , CM000674.1:g.103271232G>C | GRCh37 |
| NC_000012.10:g.101795362G>C | NCBI36 |
| NG_008690.1:g.45149C>G | |
| NG_008690.2:g.85957C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.441+8C>G MANE Select | ENSP00000448059.1:n.441+8C>G | |
| ENST00000307000.7:c.426+8C>G | ENSP00000303500.2:n.426+8C>G | |
| ENST00000549111.5:n.537+8C>G | ||
| ENST00000550978.6:c.433C>G | ||
| ENST00000551988.5:n.530+8C>G | ||
| ENST00000553106.5:c.441+8C>G | ENSP00000448059.1:n.441+8C>G | |
| NM_000277.1:c.441+8C>G | NP_000268.1:n.441+8C>G | |
| XM_011538422.1:c.441+8C>G | XP_011536724.1:n.441+8C>G | |
| NM_000277.2:c.441+8C>G | NP_000268.1:n.441+8C>G | |
| NM_001354304.1:c.441+8C>G | NP_001341233.1:n.441+8C>G | |
| XM_017019370.2:c.441+8C>G | XP_016874859.1:n.441+8C>G | |
| NM_000277.3:c.441+8C>G MANE Select | NP_000268.1:n.441+8C>G | |
| NM_001354304.2:c.441+8C>G | NP_001341233.1:n.441+8C>G |