Canonical Allele Identifier: CA2699235162
Gene:

Linked Data

dbSNP Id: rs2103801608

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722551C>T , CM000664.2:g.52722551C>T GRCh38
NC_000002.11:g.52949689C>T , CM000664.1:g.52949689C>T GRCh37
NC_000002.10:g.52803193C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.706G>A