Canonical Allele Identifier: CA1869965249
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928272T= , CM000671.2:g.104928272T= GRCh38
NC_000009.11:g.107690553T= , CM000671.1:g.107690553T= GRCh37
NC_000009.10:g.106730374T= NCBI36
NG_007981.1:g.4884A=

Transcript Alleles

HGVS Amino-acid Change
XR_930204.1:n.734+362T=
XR_930204.2:n.115+362T=