Canonical Allele Identifier: CA2555118893
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961021T>G , CM000674.2:g.29961021T>G GRCh38
NC_000012.11:g.30113954T>G , CM000674.1:g.30113954T>G GRCh37
NC_000012.10:g.30005221T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17981A>C
XR_931474.1:n.314-17981A>C
XR_931475.1:n.135-17981A>C
XR_001749060.1:n.314-17981A>C
XR_001749061.1:n.314-17981A>C