Canonical Allele Identifier: CA5839681
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs777802495
gnomAD v2: 11-5246814-G-A
gnomAD v4: 11-5225584-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225584G>A , CM000673.2:g.5225584G>A GRCh38
NC_000011.9:g.5246814G>A , CM000673.1:g.5246814G>A GRCh37
NC_000011.8:g.5203390G>A NCBI36
NG_000007.3:g.72032C>T
NG_059281.1:g.6488C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.*14C>T ENSP00000494175.1:n.*14C>T
ENST00000335295.4:c.*14C>T MANE Select ENSP00000333994.3:n.*14C>T
ENST00000633227.1:c.*274C>T ENSP00000488004.1:n.*274C>T
NM_000518.4:c.*14C>T NP_000509.1:n.*14C>T
NM_000518.5:c.*14C>T MANE Select NP_000509.1:n.*14C>T