Canonical Allele Identifier: CA851031675
Gene:

Linked Data

dbSNP Id: rs1449270797

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808208C>G , CM000670.2:g.33808208C>G GRCh38
NC_000008.10:g.33665726C>G , CM000670.1:g.33665726C>G GRCh37
NC_000008.9:g.33785268C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11772C>G
XR_002956701.1:n.240+11772C>G