Canonical Allele Identifier: CA1163450831
Gene:

Linked Data

dbSNP Id: rs1010216028

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38158491C>A , CM000663.2:g.38158491C>A GRCh38
NC_000001.10:g.38624163C>A , CM000663.1:g.38624163C>A GRCh37
NC_000001.9:g.38396750C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947202.1:n.45-3202C>A
XR_947203.1:n.61+16777C>A
XR_947204.1:n.45-3202C>A
XR_947205.1:n.45-3202C>A
XR_001737984.1:n.45-3202C>A
XR_001737985.1:n.61+16777C>A
XR_001737986.1:n.45-3202C>A
XR_001737987.1:n.45-3202C>A
XR_002958294.1:n.45-3202C>A
XR_947205.2:n.45-3202C>A