Canonical Allele Identifier: CA2529444605
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534611G>C , CM000664.2:g.41534611G>C GRCh38
NC_000002.11:g.41761751G>C , CM000664.1:g.41761751G>C GRCh37
NC_000002.10:g.41615255G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3115C>G
XR_939997.1:n.146+3115C>G
XR_939997.2:n.9529+3115C>G