Canonical Allele Identifier: CA5305725

Gene: ABO

Linked Data

• dbSNP Id: rs781814776
• ExAC: 9:136131307 C / T
• gnomAD v2: 9-136131307-C-T
• gnomAD v3: 9-133255920-C-T
• gnomAD v4: 9-133255920-C-T
• MyVariant Identifiers: chr9:g.136131307C>T (hg19) ; chr9:g.136131307_136131308delinsTG (hg19) ; chr9:g.133255920C>T (hg38) ; chr9:g.133255920_133255921delinsTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255920C>T , CM000671.2:g.133255920C>T	GRCh38
NC_000009.11:g.136131307C>T , CM000671.1:g.136131307C>T	GRCh37
NC_000009.10:g.135121128C>T	NCBI36
NG_006669.1:g.21748G>A
NG_006669.2:g.24296G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.840G>A
ENST00000647353.1:n.54-4768G>A
ENST00000679909.1:c.28+19242G>A	ENSP00000506089.1:n.28+19242G>A
ENST00000453660.3:n.822G>A
ENST00000538324.2:c.808G>A	ENSP00000483018.1:p.Gly270Arg
ENST00000611156.4:c.808G>A	ENSP00000483265.1:p.Gly270Arg
NM_020469.2:c.811G>A	NP_065202.2:p.Gly271Arg
NM_020469.3:c.811G>A	NP_065202.2:p.Gly271Arg