Canonical Allele Identifier: CA1949571829
Gene: HBB HGNC NCBI

Linked Data

dbSNP Id: rs1589893850

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227175T>G , CM000673.2:g.5227175T>G GRCh38
NC_000011.9:g.5248405T>G , CM000673.1:g.5248405T>G GRCh37
NC_000011.8:g.5204981T>G NCBI36
NG_000007.3:g.70441A>C
NG_059281.1:g.4897A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-154A>C ENSP00000494175.1:n.-154A>C
ENST00000380315.2:c.-18-136A>C ENSP00000369671.2:n.-18-136A>C