Canonical Allele Identifier: CA228572292
Gene:

Linked Data

dbSNP Id: rs181715698

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166846A>T , CM000673.2:g.112166846A>T GRCh38
NC_000011.9:g.112037569A>T , CM000673.1:g.112037569A>T GRCh37
NC_000011.8:g.111542779A>T NCBI36
NG_028143.1:g.2272T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3573A>T
ENST00000531744.5:c.315-3573A>T ENSP00000456957.1:n.315-3573A>T
ENST00000532699.1:c.315-3573A>T ENSP00000456434.1:n.315-3573A>T