Canonical Allele Identifier: CA860756251
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1376546636
MyVariant Identifiers: chr9:g.133260371G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260371G>C , CM000671.2:g.133260371G>C GRCh38
NC_000009.11:g.136135774G>C , CM000671.1:g.136135774G>C GRCh37
NC_000009.10:g.135125595G>C NCBI36
NG_006669.1:g.17279C>G
NG_006669.2:g.19844C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-505C>G
ENST00000647353.1:n.54-9219C>G
ENST00000651471.1:n.191-505C>G
ENST00000679909.1:c.28+14791C>G ENSP00000506089.1:n.28+14791C>G
ENST00000453660.3:n.168-505C>G
ENST00000538324.2:c.156-505C>G ENSP00000483018.1:n.156-505C>G
ENST00000611156.4:c.156-505C>G ENSP00000483265.1:n.156-505C>G
NM_020469.2:c.156-505C>G NP_065202.2:n.156-505C>G
NM_020469.3:c.156-505C>G NP_065202.2:n.156-505C>G
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