Canonical Allele Identifier: CA2639419276
Gene: APOH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227946C>G , CM000679.2:g.66227946C>G GRCh38
NC_000017.10:g.64224064C>G , CM000679.1:g.64224064C>G GRCh37
NC_000017.9:g.61654526C>G NCBI36
NG_012045.1:g.6493G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+74G>C MANE Select ENSP00000205948.6:n.241+74G>C
ENST00000205948.10:c.241+74G>C ENSP00000205948.6:n.241+74G>C
ENST00000577982.1:c.241+74G>C ENSP00000464301.1:n.241+74G>C
ENST00000581797.5:c.61+74G>C ENSP00000463553.1:n.61+74G>C
NM_000042.2:c.241+74G>C NP_000033.2:n.241+74G>C
NM_000042.3:c.241+74G>C MANE Select NP_000033.2:n.241+74G>C