Canonical Allele Identifier: CA1687788277
Gene:

Linked Data

dbSNP Id: rs1583217145

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.10667233T>C , CM000669.2:g.10667233T>C GRCh38
NC_000007.13:g.10706860T>C , CM000669.1:g.10706860T>C GRCh37
NC_000007.12:g.10673385T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147499.1:n.64-105656A>G
XR_001745090.1:n.376-8063T>C