Canonical Allele Identifier: CA2271191749
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs2073449361

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227947G>A , CM000679.2:g.66227947G>A GRCh38
NC_000017.10:g.64224065G>A , CM000679.1:g.64224065G>A GRCh37
NC_000017.9:g.61654527G>A NCBI36
NG_012045.1:g.6492C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+73C>T MANE Select ENSP00000205948.6:n.241+73C>T
ENST00000205948.10:c.241+73C>T ENSP00000205948.6:n.241+73C>T
ENST00000577982.1:c.241+73C>T ENSP00000464301.1:n.241+73C>T
ENST00000581797.5:c.61+73C>T ENSP00000463553.1:n.61+73C>T
NM_000042.2:c.241+73C>T NP_000033.2:n.241+73C>T
NM_000042.3:c.241+73C>T MANE Select NP_000033.2:n.241+73C>T