Canonical Allele Identifier: CA2612162217
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5225540-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225540A>C , CM000673.2:g.5225540A>C GRCh38
NC_000011.9:g.5246770A>C , CM000673.1:g.5246770A>C GRCh37
NC_000011.8:g.5203346A>C NCBI36
NG_000007.3:g.72076T>G
NG_059281.1:g.6532T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*58T>G ENSP00000494175.1:n.*58T>G
ENST00000335295.4:c.*58T>G MANE Select ENSP00000333994.3:n.*58T>G
ENST00000633227.1:c.*318T>G ENSP00000488004.1:n.*318T>G
NM_000518.4:c.*58T>G NP_000509.1:n.*58T>G
NM_000518.5:c.*58T>G MANE Select NP_000509.1:n.*58T>G