Canonical Allele Identifier: CA1258276565
Gene:

Linked Data

dbSNP Id: rs956205982

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637565T>G , CM000664.2:g.67637565T>G GRCh38
NC_000002.11:g.67864697T>G , CM000664.1:g.67864697T>G GRCh37
NC_000002.10:g.67718201T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13401A>C