Canonical Allele Identifier: CA379280279
Gene: HBG1 HGNC NCBI
HBG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.5270809A>G (hg19) chr11:g.5249579A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249579A>G , CM000673.2:g.5249579A>G GRCh38
NC_000011.9:g.5270809A>G , CM000673.1:g.5270809A>G GRCh37
NC_000011.8:g.5227385A>G NCBI36
NG_000007.3:g.48037T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000330597.5:c.104T>C (HBG1) MANE Select ENSP00000327431.4:p.Val35Ala
ENST00000642908.1:c.316-1092T>C ENSP00000495346.1:n.316-1092T>C
ENST00000647543.1:c.379-1092T>C ENSP00000496470.1:n.379-1092T>C
ENST00000648735.1:n.155T>C (HBG1)
ENST00000330597.3:c.104T>C (HBG1) ENSP00000327431.3:p.Val35Ala
ENST00000620888.4:c.316-1092T>C (HBG2) ENSP00000479637.1:n.316-1092T>C
ENST00000623781.1:c.251A>G ENSP00000485381.1:p.Asp84Gly
ENST00000632727.1:c.66T>C (HBG1) ENSP00000488759.1:p.Cys22=
NM_000559.2:c.104T>C (HBG1) NP_000550.2:p.Val35Ala
NM_000559.3:c.104T>C (HBG1) MANE Select NP_000550.2:p.Val35Ala
Search 100 bp 5'
Search 100 bp 3'