Canonical Allele Identifier: CA1283487464
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331958T= , CM000664.2:g.120331958T= GRCh38
NC_000002.11:g.121089534T= , CM000664.1:g.121089534T= GRCh37
NC_000002.10:g.120806004T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3152T= XP_011510609.1:n.141+3152T=