Canonical Allele Identifier: CA2327853204
Community Standard Title: NC_000019.10:g.21483408C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.21483408C= , CM000681.2:g.21483408C= GRCh38
NC_000019.9:g.21666210C= , CM000681.1:g.21666210C= GRCh37
NC_000019.8:g.21458050C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000600810.1:c.197-6257C= ENSP00000473166.1:n.197-6257C=