Canonical Allele Identifier: CA2492005199
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844009T= , CM000664.2:g.17844009T= GRCh38
NC_000002.11:g.18025276T= , CM000664.1:g.18025276T= GRCh37
NC_000002.10:g.17888757T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3685A=