Canonical Allele Identifier: CA2698910382
Gene:

Linked Data

dbSNP Id: rs2125217012

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844012T>C , CM000664.2:g.17844012T>C GRCh38
NC_000002.11:g.18025279T>C , CM000664.1:g.18025279T>C GRCh37
NC_000002.10:g.17888760T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3682A>G