Canonical Allele Identifier: CA2699235082
Gene:

Linked Data

dbSNP Id: rs2103801193

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722208T>C , CM000664.2:g.52722208T>C GRCh38
NC_000002.11:g.52949346T>C , CM000664.1:g.52949346T>C GRCh37
NC_000002.10:g.52802850T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.1049A>G