Canonical Allele Identifier: CA2293960073
Gene:

Linked Data

dbSNP Id: rs1568005672

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756499C>G , CM000680.2:g.31756499C>G GRCh38
NC_000018.9:g.29336462C>G , CM000680.1:g.29336462C>G GRCh37
NC_000018.8:g.27590460C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5640C>G