Canonical Allele Identifier: CA501476103
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224199C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228081C>A , CM000679.2:g.66228081C>A GRCh38
NC_000017.10:g.64224199C>A , CM000679.1:g.64224199C>A GRCh37
NC_000017.9:g.61654661C>A NCBI36
NG_012045.1:g.6358G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.180G>T MANE Select ENSP00000205948.6:p.Gly60=
ENST00000205948.10:c.180G>T ENSP00000205948.6:p.Gly60=
ENST00000577982.1:c.180G>T ENSP00000464301.1:p.Gly60=
ENST00000581797.5:c.-1G>T ENSP00000463553.1:n.-1G>T
NM_000042.2:c.180G>T NP_000033.2:p.Gly60=
NM_000042.3:c.180G>T MANE Select NP_000033.2:p.Gly60=
Search 100 bp 5'
Search 100 bp 3'