Canonical Allele Identifier: CA393996012

Gene: HBA1

Linked Data

• MyVariant Identifiers: chr16:g.227382G>T (hg19) ; chr16:g.177383G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177383G>T , CM000678.2:g.177383G>T	GRCh38
NC_000016.9:g.227382G>T , CM000678.1:g.227382G>T	GRCh37
NC_000016.8:g.167382G>T	NCBI36
NG_000006.1:g.38246G>T
NG_059186.1:g.5733G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.401G>T MANE Select	ENSP00000322421.5:p.Ser134Ile
ENST00000397797.1:c.305G>T	ENSP00000380899.1:p.Ser102Ile
ENST00000472694.1:n.537G>T
NM_000558.4:c.401G>T	NP_000549.1:p.Ser134Ile
NM_000558.5:c.401G>T MANE Select	NP_000549.1:p.Ser134Ile