Canonical Allele Identifier: CA501476082
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1295326998

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228066G>A , CM000679.2:g.66228066G>A GRCh38
NC_000017.10:g.64224184G>A , CM000679.1:g.64224184G>A GRCh37
NC_000017.9:g.61654646G>A NCBI36
NG_012045.1:g.6373C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.195C>T MANE Select ENSP00000205948.6:p.Ile65=
ENST00000205948.10:c.195C>T ENSP00000205948.6:p.Ile65=
ENST00000577982.1:c.195C>T ENSP00000464301.1:p.Ile65=
ENST00000581797.5:c.15C>T ENSP00000463553.1:p.Ile5=
NM_000042.2:c.195C>T NP_000033.2:p.Ile65=
NM_000042.3:c.195C>T MANE Select NP_000033.2:p.Ile65=