Canonical Allele Identifier: CA1869965241
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928264T= , CM000671.2:g.104928264T= GRCh38
NC_000009.11:g.107690545T= , CM000671.1:g.107690545T= GRCh37
NC_000009.10:g.106730366T= NCBI36
NG_007981.1:g.4892A=

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+354T=
XR_930204.2:n.115+354T=