Canonical Allele Identifier: CA2200882785
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1902141497
gnomAD v4: 16-176694-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176694C>T , CM000678.2:g.176694C>T GRCh38
NC_000016.9:g.226693C>T , CM000678.1:g.226693C>T GRCh37
NC_000016.8:g.166693C>T NCBI36
NG_000006.1:g.37557C>T
NG_059186.1:g.5044C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.-23C>T MANE Select ENSP00000322421.5:n.-23C>T
NM_000558.4:c.-23C>T NP_000549.1:n.-23C>T
NM_000558.5:c.-23C>T MANE Select NP_000549.1:n.-23C>T