Linked Data
gnomAD v4:
12-102917278-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102917278C>T , CM000674.2:g.102917278C>T | GRCh38 |
| NC_000012.11:g.103311056C>T , CM000674.1:g.103311056C>T | GRCh37 |
| NC_000012.10:g.101835186C>T | NCBI36 |
| NG_008690.1:g.5325G>A | |
| NG_008690.2:g.46133G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546708.5:n.493-53G>A | ||
| ENST00000546844.1:c.-95-53G>A | ENSP00000446658.1:n.-95-53G>A | |
| ENST00000547319.1:n.217-53G>A | ||
| ENST00000551337.5:c.-95-53G>A | ENSP00000447620.1:n.-95-53G>A | |
| ENST00000553106.5:c.-148G>A | ENSP00000448059.1:n.-148G>A | |
| ENST00000635500.1:n.29-4380G>A | ||
| NM_000277.1:c.-148G>A | NP_000268.1:n.-148G>A | |
| NM_000277.2:c.-148G>A | NP_000268.1:n.-148G>A | |
| NM_001354304.1:c.-95-53G>A | NP_001341233.1:n.-95-53G>A | |
| NM_001354304.2:c.-95-53G>A | NP_001341233.1:n.-95-53G>A |