Canonical Allele Identifier: CA2547293729
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216604T>G , CM000664.2:g.218216604T>G GRCh38
NC_000002.11:g.219081327T>G , CM000664.1:g.219081327T>G GRCh37
NC_000002.10:g.218789572T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.341A>C
XR_923908.1:n.338A>C