Canonical Allele Identifier: CA1672982834
Community Standard Title: NC_000006.12:g.151636579C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151636579C= , CM000668.2:g.151636579C= GRCh38
NC_000006.11:g.151957714C= , CM000668.1:g.151957714C= GRCh37
NC_000006.10:g.151999407C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+6597C=