Canonical Allele Identifier: CA2492005213
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844069T= , CM000664.2:g.17844069T= GRCh38
NC_000002.11:g.18025336T= , CM000664.1:g.18025336T= GRCh37
NC_000002.10:g.17888817T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3625A=