Canonical Allele Identifier: CA379280214

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5249555A>C , CM000673.2:g.5249555A>C GRCh38
NC_000011.9:g.5270785A>C , CM000673.1:g.5270785A>C GRCh37
NC_000011.8:g.5227361A>C NCBI36
NG_000007.3:g.48061T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330597.5:c.128T>G (HBG1) MANE Select ENSP00000327431.4:p.Phe43Cys
ENST00000642908.1:c.316-1068T>G ENSP00000495346.1:n.316-1068T>G
ENST00000647543.1:c.379-1068T>G ENSP00000496470.1:n.379-1068T>G
ENST00000648735.1:n.179T>G (HBG1)
ENST00000330597.3:c.128T>G (HBG1) ENSP00000327431.3:p.Phe43Cys
ENST00000620888.4:c.316-1068T>G (HBG2) ENSP00000479637.1:n.316-1068T>G
ENST00000623781.1:c.227A>C ENSP00000485381.1:p.Lys76Thr
ENST00000632727.1:c.90T>G (HBG1) ENSP00000488759.1:p.Leu30=
NM_000559.2:c.128T>G (HBG1) NP_000550.2:p.Phe43Cys
NM_000559.3:c.128T>G (HBG1) MANE Select NP_000550.2:p.Phe43Cys