Canonical Allele Identifier: CA1910164285
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.52573815T>A , CM000672.2:g.52573815T>A GRCh38
NC_000010.10:g.54333575T>A , CM000672.1:g.54333575T>A GRCh37
NC_000010.9:g.54003581T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945961.1:n.379-12700A>T
XR_945962.1:n.383-12700A>T
NR_155748.1:n.96-12700A>T
XR_001747449.2:n.108-12700A>T
XR_001747450.2:n.329-12700A>T
XR_945961.3:n.9426-12700A>T
XR_945962.3:n.9430-12700A>T