Canonical Allele Identifier: CA2692330852

Gene: ABO

Linked Data

• gnomAD v4: 9-133258200-G-GCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258201_133258202insCC , CM000671.2:g.133258201_133258202insCC	GRCh38
NC_000009.11:g.136133592_136133593insCC , CM000671.1:g.136133592_136133593insCC	GRCh37
NC_000009.10:g.135123413_135123414insCC	NCBI36
NG_006669.1:g.19462_19463insGG
NG_006669.2:g.22014_22015insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-69_234-68insGG
ENST00000647353.1:n.54-7049_54-7048insGG
ENST00000651471.1:n.239-69_239-68insGG
ENST00000679909.1:c.28+16961_28+16962insGG	ENSP00000506089.1:n.28+16961_28+16962insGG
ENST00000453660.3:n.216-69_216-68insGG
ENST00000538324.2:c.204-69_204-68insGG	ENSP00000483018.1:n.204-69_204-68insGG
ENST00000611156.4:c.204-69_204-68insGG	ENSP00000483265.1:n.204-69_204-68insGG
NM_020469.2:c.204-69_204-68insGG	NP_065202.2:n.204-69_204-68insGG
NM_020469.3:c.204-69_204-68insGG	NP_065202.2:n.204-69_204-68insGG