Canonical Allele Identifier: CA501476408
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073471882
MyVariant Identifiers: chr17:g.64227318A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66231200A>G , CM000679.2:g.66231200A>G GRCh38
NC_000017.10:g.64227318A>G , CM000679.1:g.64227318A>G GRCh37
NC_000017.9:g.61657780A>G NCBI36
NG_012045.1:g.3239T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-1778T>C ENSP00000464301.1:n.-43-1778T>C
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