Canonical Allele Identifier: CA1751418967
Gene:

Linked Data

dbSNP Id: rs1801696457

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807203A>T , CM000669.2:g.148807203A>T GRCh38
NC_000007.13:g.148504295A>T , CM000669.1:g.148504295A>T GRCh37
NC_000007.12:g.148135228A>T NCBI36
NG_032043.1:g.82147T>A , LRG_531:g.82147T>A

Transcript Alleles

HGVS Amino-acid Change
XR_928101.1:n.515+2118A>T
XR_928102.1:n.722+2118A>T