Canonical Allele Identifier: CA1438734808
Community Standard Title: NC_000004.12:g.11709608T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11709608T= , CM000666.2:g.11709608T= GRCh38
NC_000004.11:g.11711232T= , CM000666.1:g.11711232T= GRCh37
NC_000004.10:g.11320330T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741361.1:n.1027-53851T=