Canonical Allele Identifier: CA1905919953
Gene:

Linked Data

dbSNP Id: rs1454365948

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318503A>T , CM000672.2:g.43318503A>T GRCh38
NC_000010.10:g.43813951A>T , CM000672.1:g.43813951A>T GRCh37
NC_000010.9:g.43133957A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.16A>T
XR_945902.2:n.106A>T