Canonical Allele Identifier: CA1665740966
Gene: HBS1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.135097778A= , CM000668.2:g.135097778A= GRCh38
NC_000006.11:g.135418916A= , CM000668.1:g.135418916A= GRCh37
NC_000006.10:g.135460609A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529882.5:c.88+5150T= ENSP00000433030.1:n.88+5150T=