Canonical Allele Identifier: CA1661879307
Community Standard Title: NC_000006.12:g.126645162T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.126645162T= , CM000668.2:g.126645162T= GRCh38
NC_000006.11:g.126966308T= , CM000668.1:g.126966308T= GRCh37
NC_000006.10:g.127008001T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650727.1:n.1167-23289A=
ENST00000651326.1:n.694-41697A=
ENST00000652545.1:n.1477-23289A=