Canonical Allele Identifier: CA2699235084
Gene:

Linked Data

dbSNP Id: rs2103801219

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722236G>A , CM000664.2:g.52722236G>A GRCh38
NC_000002.11:g.52949374G>A , CM000664.1:g.52949374G>A GRCh37
NC_000002.10:g.52802878G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959384.1:n.1021C>T