Canonical Allele Identifier: CA2692330767

Gene: ABO

Linked Data

• gnomAD v4: 9-133258000-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258004del , CM000671.2:g.133258004del	GRCh38
NC_000009.11:g.136133394del , CM000671.1:g.136133394del	GRCh37
NC_000009.10:g.135123215del	NCBI36
NG_006669.1:g.19663del
NG_006669.2:g.22214del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+96del
ENST00000647353.1:n.54-6849del
ENST00000651471.1:n.329+41del
ENST00000679909.1:c.28+17161del	ENSP00000506089.1:n.28+17161del
ENST00000453660.3:n.251+96del
ENST00000538324.2:c.239+96del	ENSP00000483018.1:n.239+96del
ENST00000611156.4:c.239+96del	ENSP00000483265.1:n.239+96del
NM_020469.2:c.239+96del	NP_065202.2:n.239+96del
NM_020469.3:c.239+96del	NP_065202.2:n.239+96del