Canonical Allele Identifier: CA2630739394
Gene: HBA1 HGNC NCBI

Linked Data

gnomAD v4: 16-176877-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176877C>T , CM000678.2:g.176877C>T GRCh38
NC_000016.9:g.226876C>T , CM000678.1:g.226876C>T GRCh37
NC_000016.8:g.166876C>T NCBI36
NG_000006.1:g.37740C>T
NG_059186.1:g.5227C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.96-52C>T MANE Select ENSP00000322421.5:n.96-52C>T
ENST00000397797.1:c.-1-52C>T ENSP00000380899.1:n.-1-52C>T
ENST00000472694.1:n.180C>T
ENST00000487791.1:n.65-52C>T
NM_000558.4:c.96-52C>T NP_000549.1:n.96-52C>T
NM_000558.5:c.96-52C>T MANE Select NP_000549.1:n.96-52C>T
Search 100 bp 5'
Search 100 bp 3'