Canonical Allele Identifier: CA2467782736
Gene:

Linked Data

dbSNP Id: rs113313554

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.624523C>T , CM000686.2:g.624523C>T GRCh38
NC_000024.9:g.535258C>T , CM000686.1:g.535258C>T GRCh37
NC_000024.8:g.505258C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000711143.1:c.-512C>T ENSP00000518641.1:n.-512C>T
ENST00000711145.1:c.-512C>T ENSP00000518642.1:n.-512C>T