Canonical Allele Identifier: CA400683825
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224223C>G (hg19) chr17:g.66228105C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228105C>G , CM000679.2:g.66228105C>G GRCh38
NC_000017.10:g.64224223C>G , CM000679.1:g.64224223C>G GRCh37
NC_000017.9:g.61654685C>G NCBI36
NG_012045.1:g.6334G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.156G>C MANE Select ENSP00000205948.6:p.Lys52Asn
ENST00000205948.10:c.156G>C ENSP00000205948.6:p.Lys52Asn
ENST00000577982.1:c.156G>C ENSP00000464301.1:p.Lys52Asn
ENST00000581797.5:c.-25G>C ENSP00000463553.1:n.-25G>C
NM_000042.2:c.156G>C NP_000033.2:p.Lys52Asn
NM_000042.3:c.156G>C MANE Select NP_000033.2:p.Lys52Asn
Search 100 bp 5'
Search 100 bp 3'