Canonical Allele Identifier: CA1841175535
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551362T>G , CM000671.2:g.25551362T>G GRCh38
NC_000009.11:g.25551360T>G , CM000671.1:g.25551360T>G GRCh37
NC_000009.10:g.25541360T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-790A>C
XR_929525.2:n.674-790A>C