Canonical Allele Identifier: CA10695788
Gene:

Linked Data

dbSNP Id: rs2179652

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800696C>T , CM000663.2:g.192800696C>T GRCh38
NC_000001.10:g.192769826C>T , CM000663.1:g.192769826C>T GRCh37
NC_000001.9:g.191036449C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.126C>T