Canonical Allele Identifier: CA293118538

Gene: APOH

Linked Data

• dbSNP Id: rs991987450
• gnomAD v2: 17-64224324-G-C
• gnomAD v3: 17-66228206-G-C
• gnomAD v4: 17-66228206-G-C
• MyVariant Identifiers: chr17:g.64224324G>C (hg19) ; chr17:g.66228206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228206G>C , CM000679.2:g.66228206G>C	GRCh38
NC_000017.10:g.64224324G>C , CM000679.1:g.64224324G>C	GRCh37
NC_000017.9:g.61654786G>C	NCBI36
NG_012045.1:g.6233C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-10C>G MANE Select	ENSP00000205948.6:n.65-10C>G
ENST00000205948.10:c.65-10C>G	ENSP00000205948.6:n.65-10C>G
ENST00000577982.1:c.65-10C>G	ENSP00000464301.1:n.65-10C>G
ENST00000581797.5:c.-116-10C>G	ENSP00000463553.1:n.-116-10C>G
NM_000042.2:c.65-10C>G	NP_000033.2:n.65-10C>G
NM_000042.3:c.65-10C>G MANE Select	NP_000033.2:n.65-10C>G