Canonical Allele Identifier: CA379273693
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225663C>A , CM000673.2:g.5225663C>A GRCh38
NC_000011.9:g.5246893C>A , CM000673.1:g.5246893C>A GRCh37
NC_000011.8:g.5203469C>A NCBI36
NG_000007.3:g.71953G>T
NG_059281.1:g.6409G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.379G>T ENSP00000494175.1:p.Val127Leu
ENST00000335295.4:c.379G>T MANE Select ENSP00000333994.3:p.Val127Leu
ENST00000475226.1:n.311G>T
ENST00000633227.1:c.*195G>T ENSP00000488004.1:n.*195G>T
NM_000518.4:c.379G>T NP_000509.1:p.Val127Leu
NM_000518.5:c.379G>T MANE Select NP_000509.1:p.Val127Leu