Canonical Allele Identifier: CA1804794203
Gene:

Linked Data

dbSNP Id: rs1810398057

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269627G>A , CM000670.2:g.97269627G>A GRCh38
NC_000008.10:g.98281855G>A , CM000670.1:g.98281855G>A GRCh37
NC_000008.9:g.98351031G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149443C>T