Canonical Allele Identifier: CA2491383598
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458174T= , CM000664.2:g.16458174T= GRCh38
NC_000002.11:g.16639442T= , CM000664.1:g.16639442T= GRCh37
NC_000002.10:g.16502923T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939752.1:n.396-3080A=