Canonical Allele Identifier: CA2777483239
Gene:

Genomic Alleles

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

Transcript Alleles

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