Canonical Allele Identifier: CA375685775

Gene: ABO

Linked Data

• gnomAD v4: 9-133256083-G-T
• MyVariant Identifiers: chr9:g.136131470G>T (hg19) ; chr9:g.133256083G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256083G>T , CM000671.2:g.133256083G>T	GRCh38
NC_000009.11:g.136131470G>T , CM000671.1:g.136131470G>T	GRCh37
NC_000009.10:g.135121291G>T	NCBI36
NG_006669.1:g.21585C>A
NG_006669.2:g.24133C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.677C>A
ENST00000647353.1:n.54-4931C>A
ENST00000679909.1:c.28+19079C>A	ENSP00000506089.1:n.28+19079C>A
ENST00000453660.3:n.659C>A
ENST00000538324.2:c.645C>A	ENSP00000483018.1:p.Phe215Leu
ENST00000611156.4:c.645C>A	ENSP00000483265.1:p.Phe215Leu
NM_020469.2:c.648C>A	NP_065202.2:p.Phe216Leu
NM_020469.3:c.648C>A	NP_065202.2:p.Phe216Leu