Canonical Allele Identifier: CA1672979069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633533T= , CM000668.2:g.151633533T= GRCh38
NC_000006.11:g.151954668T= , CM000668.1:g.151954668T= GRCh37
NC_000006.10:g.151996361T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3551T=