Canonical Allele Identifier: CA1672979251
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633704C= , CM000668.2:g.151633704C= GRCh38
NC_000006.11:g.151954839C= , CM000668.1:g.151954839C= GRCh37
NC_000006.10:g.151996532C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3722C=