Canonical Allele Identifier: CA1665744973
Gene: HBS1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.135102071T= , CM000668.2:g.135102071T= GRCh38
NC_000006.11:g.135423209T= , CM000668.1:g.135423209T= GRCh37
NC_000006.10:g.135464902T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529882.5:c.88+857A= ENSP00000433030.1:n.88+857A=