Canonical Allele Identifier: CA1735257891
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.112988322C= , CM000669.2:g.112988322C= GRCh38
NC_000007.13:g.112628377C= , CM000669.1:g.112628377C= GRCh37
NC_000007.12:g.112415613C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110162.1:n.77-1658G=