Canonical Allele Identifier: CA1880834240
Gene:

Linked Data

dbSNP Id: rs1829777612

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576732G>A , CM000671.2:g.129576732G>A GRCh38
NC_000009.11:g.132339011G>A , CM000671.1:g.132339011G>A GRCh37
NC_000009.10:g.131378832G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1134G>A