Canonical Allele Identifier: CA15605178
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21701433T>C , CM000671.2:g.21701433T>C GRCh38
NC_000009.11:g.21701432T>C , CM000671.1:g.21701432T>C GRCh37
NC_000009.10:g.21691432T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.384+1484A>G