Canonical Allele Identifier: CA375686301

Gene: ABO

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256265G>A , CM000671.2:g.133256265G>A	GRCh38
NC_000009.11:g.136131652G>A , CM000671.1:g.136131652G>A	GRCh37
NC_000009.10:g.135121473G>A	NCBI36
NG_006669.1:g.21403C>T
NG_006669.2:g.23951C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.495C>T
ENST00000647353.1:n.54-5113C>T
ENST00000651471.1:n.421C>T
ENST00000679909.1:c.28+18897C>T	ENSP00000506089.1:n.28+18897C>T
ENST00000453660.3:n.477C>T
ENST00000538324.2:c.463C>T	ENSP00000483018.1:p.Pro155Ser
ENST00000611156.4:c.463C>T	ENSP00000483265.1:p.Pro155Ser
NM_020469.2:c.466C>T	NP_065202.2:p.Pro156Ser
NM_020469.3:c.466C>T	NP_065202.2:p.Pro156Ser