Canonical Allele Identifier: CA10745275
Gene:

Linked Data

dbSNP Id: rs10911021

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182112825C>T , CM000663.2:g.182112825C>T GRCh38
NC_000001.10:g.182081960C>T , CM000663.1:g.182081960C>T GRCh37
NC_000001.9:g.180348583C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922341.1:n.243-2426C>T
XR_922341.2:n.334-2426C>T