Canonical Allele Identifier: CA393995998
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.227372G>C (hg19) chr16:g.177373G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177373G>C , CM000678.2:g.177373G>C GRCh38
NC_000016.9:g.227372G>C , CM000678.1:g.227372G>C GRCh37
NC_000016.8:g.167372G>C NCBI36
NG_000006.1:g.38236G>C
NG_059186.1:g.5723G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.391G>C MANE Select ENSP00000322421.5:p.Ala131Pro
ENST00000397797.1:c.295G>C ENSP00000380899.1:p.Ala99Pro
ENST00000472694.1:n.527G>C
NM_000558.4:c.391G>C NP_000549.1:p.Ala131Pro
NM_000558.5:c.391G>C MANE Select NP_000549.1:p.Ala131Pro
Search 100 bp 5'
Search 100 bp 3'