Canonical Allele Identifier: CA1839056761
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756115T= , CM000671.2:g.21756115T= GRCh38
NC_000009.11:g.21756114T= , CM000671.1:g.21756114T= GRCh37
NC_000009.10:g.21746114T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11710A=