Canonical Allele Identifier: CA916083231
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869288
ClinVar RCV Id: RCV001078340
dbSNP Id: rs34598529

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227100T>G , CM000673.2:g.5227100T>G GRCh38
NC_000011.9:g.5248330T>G , CM000673.1:g.5248330T>G GRCh37
NC_000011.8:g.5204906T>G NCBI36
NG_000007.3:g.70516A>C
NG_059281.1:g.4972A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-79A>C ENSP00000494175.1:n.-79A>C
ENST00000380315.2:c.-18-61A>C ENSP00000369671.2:n.-18-61A>C