Canonical Allele Identifier: CA1283487449
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331917C= , CM000664.2:g.120331917C= GRCh38
NC_000002.11:g.121089493C= , CM000664.1:g.121089493C= GRCh37
NC_000002.10:g.120805963C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3111C= XP_011510609.1:n.141+3111C=