Canonical Allele Identifier: CA400683948
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1567743212
MyVariant Identifiers: chr17:g.64224278A>C (hg19) chr17:g.66228160A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228160A>C , CM000679.2:g.66228160A>C GRCh38
NC_000017.10:g.64224278A>C , CM000679.1:g.64224278A>C GRCh37
NC_000017.9:g.61654740A>C NCBI36
NG_012045.1:g.6279T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.101T>G MANE Select ENSP00000205948.6:p.Val34Gly
ENST00000205948.10:c.101T>G ENSP00000205948.6:p.Val34Gly
ENST00000577982.1:c.101T>G ENSP00000464301.1:p.Val34Gly
ENST00000581797.5:c.-80T>G ENSP00000463553.1:n.-80T>G
NM_000042.2:c.101T>G NP_000033.2:p.Val34Gly
NM_000042.3:c.101T>G MANE Select NP_000033.2:p.Val34Gly
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Search 100 bp 3'