Canonical Allele Identifier: CA2388529170
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37560476T>G , CM000683.2:g.37560476T>G GRCh38
NC_000021.8:g.38932778T>G , CM000683.1:g.38932778T>G GRCh37
NC_000021.7:g.37854648T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017028523.1:c.-2950T>G XP_016884012.1:n.-2950T>G
XR_937706.2:n.458T>G
XR_005647073.1:n.458T>G