Canonical Allele Identifier: CA2579829116
Gene: HBB HGNC NCBI

Linked Data

gnomAD v4: 11-5227076-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227076A>G , CM000673.2:g.5227076A>G GRCh38
NC_000011.9:g.5248306A>G , CM000673.1:g.5248306A>G GRCh37
NC_000011.8:g.5204882A>G NCBI36
NG_000007.3:g.70540T>C
NG_059281.1:g.4996T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-55T>C ENSP00000494175.1:n.-55T>C
ENST00000380315.2:c.-18-37T>C ENSP00000369671.2:n.-18-37T>C