Canonical Allele Identifier: CA1949563966
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225579G= , CM000673.2:g.5225579G= GRCh38
NC_000011.9:g.5246809G= , CM000673.1:g.5246809G= GRCh37
NC_000011.8:g.5203385G= NCBI36
NG_000007.3:g.72037C=
NG_059281.1:g.6493C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*19C= ENSP00000494175.1:n.*19C=
ENST00000335295.4:c.*19C= MANE Select ENSP00000333994.3:n.*19C=
ENST00000633227.1:c.*279C= ENSP00000488004.1:n.*279C=
NM_000518.4:c.*19C= NP_000509.1:n.*19C=
NM_000518.5:c.*19C= MANE Select NP_000509.1:n.*19C=