Canonical Allele Identifier: CA11180739
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21088669T>G , CM000664.2:g.21088669T>G GRCh38
NC_000002.11:g.21311541T>G , CM000664.1:g.21311541T>G GRCh37
NC_000002.10:g.21165046T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939796.1:n.193-7452T>G
XR_939797.1:n.193-7452T>G