Canonical Allele Identifier: CA400683753
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000205948.11:c.195C>G MANE Select ENSP00000205948.6:p.Ile65Met
ENST00000205948.10:c.195C>G ENSP00000205948.6:p.Ile65Met
ENST00000577982.1:c.195C>G ENSP00000464301.1:p.Ile65Met
ENST00000581797.5:c.15C>G ENSP00000463553.1:p.Ile5Met
NM_000042.2:c.195C>G NP_000033.2:p.Ile65Met
NM_000042.3:c.195C>G MANE Select NP_000033.2:p.Ile65Met