Canonical Allele Identifier: CA259369490
Gene:

Linked Data

dbSNP Id: rs571948908

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384951A>G , CM000676.2:g.36384951A>G GRCh38
NC_000014.8:g.36854156A>G , CM000676.1:g.36854156A>G GRCh37
NC_000014.7:g.35923907A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12208A>G XP_011535730.1:n.319-12208A>G
XR_943756.1:n.358+23855A>G