Canonical Allele Identifier: CA1804794240
Gene:

Linked Data

dbSNP Id: rs1810398842

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269685G>A , CM000670.2:g.97269685G>A GRCh38
NC_000008.10:g.98281913G>A , CM000670.1:g.98281913G>A GRCh37
NC_000008.9:g.98351089G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149385C>T