Canonical Allele Identifier: CA492994543
Gene: HBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.227021G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177022G>C , CM000678.2:g.177022G>C GRCh38
NC_000016.9:g.227021G>C , CM000678.1:g.227021G>C GRCh37
NC_000016.8:g.167021G>C NCBI36
NG_000006.1:g.37885G>C
NG_059186.1:g.5372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.189G>C MANE Select ENSP00000322421.5:p.Val63=
ENST00000397797.1:c.93G>C ENSP00000380899.1:p.Val31=
ENST00000472694.1:n.325G>C
ENST00000487791.1:n.158G>C
NM_000558.4:c.189G>C NP_000549.1:p.Val63=
NM_000558.5:c.189G>C MANE Select NP_000549.1:p.Val63=
Search 100 bp 5'
Search 100 bp 3'