Canonical Allele Identifier: CA1735257922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.112988405C= , CM000669.2:g.112988405C= GRCh38
NC_000007.13:g.112628460C= , CM000669.1:g.112628460C= GRCh37
NC_000007.12:g.112415696C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110162.1:n.77-1741G=