Canonical Allele Identifier: CA393995140
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.226989T>C (hg19) chr16:g.176990T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176990T>C , CM000678.2:g.176990T>C GRCh38
NC_000016.9:g.226989T>C , CM000678.1:g.226989T>C GRCh37
NC_000016.8:g.166989T>C NCBI36
NG_000006.1:g.37853T>C
NG_059186.1:g.5340T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.157T>C MANE Select ENSP00000322421.5:p.Ser53Pro
ENST00000397797.1:c.61T>C ENSP00000380899.1:p.Ser21Pro
ENST00000472694.1:n.293T>C
ENST00000487791.1:n.126T>C
NM_000558.4:c.157T>C NP_000549.1:p.Ser53Pro
NM_000558.5:c.157T>C MANE Select NP_000549.1:p.Ser53Pro
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