Canonical Allele Identifier: CA1283487502
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332056A= , CM000664.2:g.120332056A= GRCh38
NC_000002.11:g.121089632A= , CM000664.1:g.121089632A= GRCh37
NC_000002.10:g.120806102A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3250A= XP_011510609.1:n.141+3250A=