Linked Data
dbSNP Id:
rs13096142
gnomAD v2:
3-46281744-C-T
gnomAD v3:
3-46240253-C-T
gnomAD v4:
3-46240253-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46240253C>T , CM000665.2:g.46240253C>T | GRCh38 |
| NC_000003.11:g.46281744C>T , CM000665.1:g.46281744C>T | GRCh37 |
| NC_000003.10:g.46256748C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357422.2:c.-67-2149C>T | ENSP00000350003.2:n.-67-2149C>T | |
| XM_006712960.2:c.-67-2149C>T | XP_006713023.1:n.-67-2149C>T | |
| XM_011533334.1:c.-154-2149C>T | XP_011531636.1:n.-154-2149C>T | |
| XM_011533335.1:c.-148-2149C>T | XP_011531637.1:n.-148-2149C>T | |
| XM_006712960.3:c.-67-2149C>T | XP_006713023.1:n.-67-2149C>T | |
| XM_011533335.2:c.-148-2149C>T | XP_011531637.1:n.-148-2149C>T | |
| XM_017005686.1:c.-965-2149C>T | XP_016861175.1:n.-965-2149C>T |