Canonical Allele Identifier: CA1697903785
Gene:

Linked Data

dbSNP Id: rs1791156704

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911453C>T , CM000669.2:g.30911453C>T GRCh38
NC_000007.13:g.30951068C>T , CM000669.1:g.30951068C>T GRCh37
NC_000007.12:g.30917593C>T NCBI36
NG_007475.2:g.63060C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-540C>T