Canonical Allele Identifier: CA379280327

Gene: HBG1 HBG2

Linked Data

• dbSNP Id: rs1589906512
• MyVariant Identifiers: chr11:g.5270940T>G (hg19) ; chr11:g.5249710T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249710T>G , CM000673.2:g.5249710T>G	GRCh38
NC_000011.9:g.5270940T>G , CM000673.1:g.5270940T>G	GRCh37
NC_000011.8:g.5227516T>G	NCBI36
NG_000007.3:g.47906A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330597.5:c.92+3A>C (HBG1) MANE Select	ENSP00000327431.4:n.92+3A>C
ENST00000642908.1:c.316-1223A>C	ENSP00000495346.1:n.316-1223A>C
ENST00000647543.1:c.379-1223A>C	ENSP00000496470.1:n.379-1223A>C
ENST00000648735.1:n.143+3A>C (HBG1)
ENST00000330597.3:c.92+3A>C (HBG1)	ENSP00000327431.3:n.92+3A>C
ENST00000620888.4:c.316-1223A>C (HBG2)	ENSP00000479637.1:n.316-1223A>C
ENST00000623781.1:c.265-2T>G	ENSP00000485381.1:n.265-2T>G
ENST00000632727.1:c.54+41A>C (HBG1)	ENSP00000488759.1:n.54+41A>C
NM_000559.2:c.92+3A>C (HBG1)	NP_000550.2:n.92+3A>C
NM_000559.3:c.92+3A>C (HBG1) MANE Select	NP_000550.2:n.92+3A>C