Canonical Allele Identifier: CA217123990

Gene: HBD

Linked Data

• dbSNP Id: rs200264296
• MyVariant Identifiers: chr11:g.5255396C>A (hg19) ; chr11:g.5234166C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5234166C>A , CM000673.2:g.5234166C>A	GRCh38
NC_000011.9:g.5255396C>A , CM000673.1:g.5255396C>A	GRCh37
NC_000011.8:g.5211972C>A	NCBI36
NG_000007.3:g.63450G>T
NG_063112.2:g.14492G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000643122.1:c.140G>T	ENSP00000494708.1:p.Gly47Val
ENST00000650601.1:c.140G>T MANE Select	ENSP00000497529.1:p.Gly47Val
ENST00000292901.7:c.140G>T	ENSP00000292901.3:p.Gly47Val
ENST00000380299.3:c.140G>T	ENSP00000369654.3:p.Gly47Val
ENST00000417377.1:c.92+176G>T	ENSP00000414741.1:n.92+176G>T
ENST00000429817.1:c.140G>T	ENSP00000393810.1:p.Gly47Val
NM_000519.3:c.140G>T	NP_000510.1:p.Gly47Val
NM_000519.4:c.140G>T MANE Select	NP_000510.1:p.Gly47Val