Canonical Allele Identifier: CA1328655602
Gene:

Linked Data

dbSNP Id: rs1689247075

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216601A>G , CM000664.2:g.218216601A>G GRCh38
NC_000002.11:g.219081324A>G , CM000664.1:g.219081324A>G GRCh37
NC_000002.10:g.218789569A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_241416.2:n.344T>C
XR_923908.1:n.341T>C