Canonical Allele Identifier: CA1895825828
Gene:

Linked Data

dbSNP Id: rs7072776

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21744013A>T , CM000672.2:g.21744013A>T GRCh38
NC_000010.10:g.22032942A>T , CM000672.1:g.22032942A>T GRCh37
NC_000010.9:g.22072948A>T NCBI36
NG_027818.1:g.214842A>T
NG_027818.2:g.214842A>T

Transcript Alleles

HGVS Amino-acid change
XR_001747388.1:n.1010+6427T>A