Canonical Allele Identifier: CA375682218

Gene: ABO

Linked Data

• gnomAD v4: 9-133255624-G-A
• MyVariant Identifiers: chr9:g.136131011G>A (hg19) ; chr9:g.133255624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255624G>A , CM000671.2:g.133255624G>A	GRCh38
NC_000009.11:g.136131011G>A , CM000671.1:g.136131011G>A	GRCh37
NC_000009.10:g.135120832G>A	NCBI36
NG_006669.1:g.22044C>T
NG_006669.2:g.24592C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1136C>T
ENST00000647353.1:n.54-4472C>T
ENST00000679909.1:c.28+19538C>T	ENSP00000506089.1:n.28+19538C>T
ENST00000453660.3:n.1118C>T
ENST00000538324.2:c.1100C>T	ENSP00000483018.1:p.Ser367Phe
ENST00000611156.4:c.*42C>T	ENSP00000483265.1:n.*42C>T
NM_020469.2:c.*42C>T	NP_065202.2:n.*42C>T
NM_020469.3:c.*42C>T	NP_065202.2:n.*42C>T