Canonical Allele Identifier: CA2087969103
Community Standard Title: NC_000013.11:g.43897741A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.43897741A= , CM000675.2:g.43897741A= GRCh38
NC_000013.10:g.44471877A= , CM000675.1:g.44471877A= GRCh37
NC_000013.9:g.43369877A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000627615.1:c.756+6171A=