Canonical Allele Identifier: CA1283487441
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331888G= , CM000664.2:g.120331888G= GRCh38
NC_000002.11:g.121089464G= , CM000664.1:g.121089464G= GRCh37
NC_000002.10:g.120805934G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3082G= XP_011510609.1:n.141+3082G=