Canonical Allele Identifier: CA2612161496
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5225836-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225836G>C , CM000673.2:g.5225836G>C GRCh38
NC_000011.9:g.5247066G>C , CM000673.1:g.5247066G>C GRCh37
NC_000011.8:g.5203642G>C NCBI36
NG_000007.3:g.71780C>G
NG_059281.1:g.6236C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.316-110C>G ENSP00000494175.1:n.316-110C>G
ENST00000335295.4:c.316-110C>G MANE Select ENSP00000333994.3:n.316-110C>G
ENST00000475226.1:n.248-110C>G
ENST00000633227.1:c.*132-110C>G ENSP00000488004.1:n.*132-110C>G
NM_000518.4:c.316-110C>G NP_000509.1:n.316-110C>G
NM_000518.5:c.316-110C>G MANE Select NP_000509.1:n.316-110C>G