Canonical Allele Identifier: CA1283487475
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331996C= , CM000664.2:g.120331996C= GRCh38
NC_000002.11:g.121089572C= , CM000664.1:g.121089572C= GRCh37
NC_000002.10:g.120806042C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3190C= XP_011510609.1:n.141+3190C=