Canonical Allele Identifier: CA1839056688
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755990C= , CM000671.2:g.21755990C= GRCh38
NC_000009.11:g.21755989C= , CM000671.1:g.21755989C= GRCh37
NC_000009.10:g.21745989C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746563.2:n.163+11835G=