Canonical Allele Identifier: CA1804794233
Gene:

Linked Data

dbSNP Id: rs1810398701

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269661C>A , CM000670.2:g.97269661C>A GRCh38
NC_000008.10:g.98281889C>A , CM000670.1:g.98281889C>A GRCh37
NC_000008.9:g.98351065C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149409G>T