Linked Data
dbSNP Id:
rs11209003
gnomAD v2:
1-67601132-G-T
gnomAD v3:
1-67135449-G-T
gnomAD v4:
1-67135449-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67135449G>T , CM000663.2:g.67135449G>T | GRCh38 |
| NC_000001.10:g.67601132G>T , CM000663.1:g.67601132G>T | GRCh37 |
| NC_000001.9:g.67373720G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371007.6:c.-103-4222C>A | ENSP00000360046.1:n.-103-4222C>A | |
| ENST00000448166.6:c.-103-4222C>A | ENSP00000415519.2:n.-103-4222C>A | |
| XM_011541466.1:c.-18+6165C>A | XP_011539768.1:n.-18+6165C>A | |
| XM_011541466.2:c.-18+6165C>A | XP_011539768.1:n.-18+6165C>A |