Canonical Allele Identifier: CA472885943
Gene: HBD HGNC NCBI

Linked Data

gnomAD v4: 11-5234054-G-A
MyVariant Identifiers: chr11:g.5255284G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5234054G>A , CM000673.2:g.5234054G>A GRCh38
NC_000011.9:g.5255284G>A , CM000673.1:g.5255284G>A GRCh37
NC_000011.8:g.5211860G>A NCBI36
NG_000007.3:g.63562C>T
NG_063112.2:g.14604C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643122.1:c.252C>T ENSP00000494708.1:p.Gly84=
ENST00000650601.1:c.252C>T MANE Select ENSP00000497529.1:p.Gly84=
ENST00000292901.7:c.252C>T ENSP00000292901.3:p.Gly84=
ENST00000380299.3:c.252C>T ENSP00000369654.3:p.Gly84=
ENST00000417377.1:c.92+288C>T ENSP00000414741.1:n.92+288C>T
ENST00000429817.1:c.252C>T ENSP00000393810.1:p.Gly84=
NM_000519.3:c.252C>T NP_000510.1:p.Gly84=
NM_000519.4:c.252C>T MANE Select NP_000510.1:p.Gly84=