Canonical Allele Identifier: CA1458307702
Community Standard Title: NC_000004.12:g.53794991A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.53794991A= , CM000666.2:g.53794991A= GRCh38
NC_000004.11:g.54661158A= , CM000666.1:g.54661158A= GRCh37
NC_000004.10:g.54355915A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000507166.5:c.1017+369026A= ENSP00000423325.1:n.1017+369026A=