Canonical Allele Identifier: CA5305793

Gene: ABO

Linked Data

• dbSNP Id: rs374698850
• ExAC: 9:136131511 C / T
• gnomAD v2: 9-136131511-C-T
• gnomAD v3: 9-133256124-C-T
• gnomAD v4: 9-133256124-C-T
• MyVariant Identifiers: chr9:g.136131511C>T (hg19) ; chr9:g.133256124C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256124C>T , CM000671.2:g.133256124C>T	GRCh38
NC_000009.11:g.136131511C>T , CM000671.1:g.136131511C>T	GRCh37
NC_000009.10:g.135121332C>T	NCBI36
NG_006669.1:g.21544G>A
NG_006669.2:g.24092G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.636G>A
ENST00000647353.1:n.54-4972G>A
ENST00000651471.1:n.562G>A
ENST00000679909.1:c.28+19038G>A	ENSP00000506089.1:n.28+19038G>A
ENST00000453660.3:n.618G>A
ENST00000538324.2:c.604G>A	ENSP00000483018.1:p.Glu202Lys
ENST00000611156.4:c.604G>A	ENSP00000483265.1:p.Glu202Lys
NM_020469.2:c.607G>A	NP_065202.2:p.Glu203Lys
NM_020469.3:c.607G>A	NP_065202.2:p.Glu203Lys