Canonical Allele Identifier: CA1804794131
Gene:

Linked Data

dbSNP Id: rs1810397374

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269571A>T , CM000670.2:g.97269571A>T GRCh38
NC_000008.10:g.98281799A>T , CM000670.1:g.98281799A>T GRCh37
NC_000008.9:g.98350975A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149499T>A