Canonical Allele Identifier: CA764892150
Gene:

Linked Data

dbSNP Id: rs1411441901

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216607G>A , CM000664.2:g.218216607G>A GRCh38
NC_000002.11:g.219081330G>A , CM000664.1:g.219081330G>A GRCh37
NC_000002.10:g.218789575G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.338C>T
XR_923908.1:n.335C>T