Canonical Allele Identifier: CA102638055
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs148915469

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474257A>C , CM000666.2:g.99474257A>C GRCh38
NC_000004.11:g.100395414A>C , CM000666.1:g.100395414A>C GRCh37
NC_000004.10:g.100614437A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506494.1:n.243-2395T>G