Canonical Allele Identifier: CA39048863
Gene:

Linked Data

dbSNP Id: rs10915864

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225713304A>G , CM000663.2:g.225713304A>G GRCh38
NC_000001.10:g.225901006A>G , CM000663.1:g.225901006A>G GRCh37
NC_000001.9:g.223967629A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_426933.2:n.480+2736A>G
XR_949209.1:n.481-2720A>G
XR_001738498.1:n.385+2736A>G
XR_426933.3:n.1488+2736A>G