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Canonical Allele Identifier:
CA375686301
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131652G>A (hg19)
chr9:g.133256265G>A (hg38)
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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
NM_020469.2:c.466C>T
NP_065202.2:p.Pro156Ser
NM_020469.3:c.466C>T
NP_065202.2:p.Pro156Ser
ENST00000453660.3:n.477C>T
ENST00000538324.2:c.463C>T
ENSP00000483018.1:p.Pro155Ser
ENST00000611156.4:c.463C>T
ENSP00000483265.1:p.Pro155Ser
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