Canonical Allele Identifier: CA1804794676
Community Standard Title: NC_000008.11:g.97269961G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269961G= , CM000670.2:g.97269961G= GRCh38
NC_000008.10:g.98282189G= , CM000670.1:g.98282189G= GRCh37
NC_000008.9:g.98351365G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149109C=