Canonical Allele Identifier: CA1282456452
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079680A= , CM000664.2:g.118079680A= GRCh38
NC_000002.11:g.118837256A= , CM000664.1:g.118837256A= GRCh37
NC_000002.10:g.118553726A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2148T= XP_011510607.1:n.697-2148T=
XR_001739662.2:n.138+8571T=