Canonical Allele Identifier: CA2056175895
Community Standard Title: NC_000012.12:g.95318100A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95318100A= , CM000674.2:g.95318100A= GRCh38
NC_000012.11:g.95711876A= , CM000674.1:g.95711876A= GRCh37
NC_000012.10:g.94236007A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000636165.1:n.1059-6646T=