Canonical Allele Identifier: CA393995849
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs34863047
gnomAD v3: 16-177316-G-T
gnomAD v4: 16-177316-G-T
MyVariant Identifiers: chr16:g.227315G>T (hg19) chr16:g.177316G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177316G>T , CM000678.2:g.177316G>T GRCh38
NC_000016.9:g.227315G>T , CM000678.1:g.227315G>T GRCh37
NC_000016.8:g.167315G>T NCBI36
NG_000006.1:g.38179G>T
NG_059186.1:g.5666G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.334G>T MANE Select ENSP00000322421.5:p.Ala112Ser
ENST00000397797.1:c.238G>T ENSP00000380899.1:p.Ala80Ser
ENST00000472694.1:n.470G>T
NM_000558.4:c.334G>T NP_000549.1:p.Ala112Ser
NM_000558.5:c.334G>T MANE Select NP_000549.1:p.Ala112Ser
Search 100 bp 5'
Search 100 bp 3'