Canonical Allele Identifier: CA393995000
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176793-G-A
MyVariant Identifiers: chr16:g.226792G>A (hg19) chr16:g.176793G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176793G>A , CM000678.2:g.176793G>A GRCh38
NC_000016.9:g.226792G>A , CM000678.1:g.226792G>A GRCh37
NC_000016.8:g.166792G>A NCBI36
NG_000006.1:g.37656G>A
NG_059186.1:g.5143G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.77G>A MANE Select ENSP00000322421.5:p.Gly26Asp
ENST00000397797.1:c.-2+31G>A ENSP00000380899.1:n.-2+31G>A
ENST00000472694.1:n.96G>A
ENST00000487791.1:n.46G>A
NM_000558.4:c.77G>A NP_000549.1:p.Gly26Asp
NM_000558.5:c.77G>A MANE Select NP_000549.1:p.Gly26Asp
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Search 100 bp 3'