Canonical Allele Identifier: CA13756040
Gene:

Linked Data

dbSNP Id: rs4761659

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293308T>C , CM000674.2:g.93293308T>C GRCh38
NC_000012.11:g.93687084T>C , CM000674.1:g.93687084T>C GRCh37
NC_000012.10:g.92211215T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040096.1:n.329+34719A>G