Canonical Allele Identifier: CA677767847
Gene: HBG2 HGNC NCBI

Linked Data

dbSNP Id: rs1554921759
MyVariant Identifiers: chr11:g.5271245G>T (hg19) chr11:g.5250015G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5250015G>T , CM000673.2:g.5250015G>T GRCh38
NC_000011.9:g.5271245G>T , CM000673.1:g.5271245G>T GRCh37
NC_000011.8:g.5227821G>T NCBI36
NG_000007.3:g.47601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000642908.1:c.316-1528C>A ENSP00000495346.1:n.316-1528C>A
ENST00000647543.1:c.379-1528C>A ENSP00000496470.1:n.379-1528C>A
ENST00000620888.4:c.316-1528C>A ENSP00000479637.1:n.316-1528C>A
Search 100 bp 5'
Search 100 bp 3'