Canonical Allele Identifier: CA1818149535
Gene:

Linked Data

dbSNP Id: rs1586738736

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999549A>T , CM000670.2:g.126999549A>T GRCh38
NC_000008.10:g.128011794A>T , CM000670.1:g.128011794A>T GRCh37
NC_000008.9:g.128080976A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7006A>T