Linked Data
dbSNP Id:
rs1273593600
gnomAD v2:
16-67974484-C-T
gnomAD v3:
16-67940581-C-T
gnomAD v4:
16-67940581-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940581C>T , CM000678.2:g.67940581C>T | GRCh38 |
| NC_000016.9:g.67974484C>T , CM000678.1:g.67974484C>T | GRCh37 |
| NC_000016.8:g.66531985C>T | NCBI36 |
| NG_009778.1:g.8532G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.749-103G>A MANE Select | ENSP00000264005.5:n.749-103G>A | |
| ENST00000264005.9:c.749-103G>A | ENSP00000264005.5:n.749-103G>A | |
| ENST00000570369.5:c.156-507G>A | ||
| ENST00000570980.1:c.533-103G>A | ENSP00000464651.1:n.533-103G>A | |
| ENST00000573538.5:c.487-103G>A | ENSP00000463220.1:n.487-103G>A | |
| NM_000229.1:c.749-103G>A | NP_000220.1:n.749-103G>A | |
| NM_000229.2:c.749-103G>A MANE Select | NP_000220.1:n.749-103G>A |