Linked Data
dbSNP Id:
rs1025910491
gnomAD v2:
19-4090554-G-A
gnomAD v3:
19-4090556-G-A
gnomAD v4:
19-4090556-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4090556G>A , CM000681.2:g.4090556G>A | GRCh38 |
| NC_000019.9:g.4090554G>A , CM000681.1:g.4090554G>A | GRCh37 |
| NC_000019.8:g.4041554G>A | NCBI36 |
| NG_007996.1:g.38573C>T , LRG_750:g.38573C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.1684C>T | ||
| ENST00000688002.1:n.3396C>T | ||
| ENST00000688751.1:n.381C>T | ||
| ENST00000689792.1:n.1149C>T | ||
| ENST00000262948.10:c.*42C>T MANE Select | ENSP00000262948.4:n.*42C>T | |
| ENST00000262948.9:c.*42C>T | ENSP00000262948.3:n.*42C>T | |
| ENST00000394867.8:c.*42C>T | ENSP00000378336.1:n.*42C>T | |
| ENST00000597263.5:n.430C>T | ||
| ENST00000600584.5:n.2694C>T | ||
| ENST00000601786.5:n.1546C>T | ||
| NM_030662.3:c.*42C>T , LRG_750t1:c.*42C>T | NP_109587.1:n.*42C>T | |
| XM_006722799.2:c.*42C>T | XP_006722862.1:n.*42C>T | |
| XM_011528133.1:c.*42C>T | XP_011526435.1:n.*42C>T | |
| NM_030662.4:c.*42C>T MANE Select | NP_109587.1:n.*42C>T |