Canonical Allele Identifier: CA539586562
Gene:

Linked Data

dbSNP Id: rs1305205749

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216626C>T , CM000664.2:g.218216626C>T GRCh38
NC_000002.11:g.219081349C>T , CM000664.1:g.219081349C>T GRCh37
NC_000002.10:g.218789594C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.319G>A
XR_923908.1:n.316G>A