Canonical Allele Identifier: CA293118542

Gene: APOH

Linked Data

• dbSNP Id: rs980112213
• gnomAD v2: 17-64224377-G-A
• gnomAD v3: 17-66228259-G-A
• gnomAD v4: 17-66228259-G-A
• MyVariant Identifiers: chr17:g.64224377G>A (hg19) ; chr17:g.66228259G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228259G>A , CM000679.2:g.66228259G>A	GRCh38
NC_000017.10:g.64224377G>A , CM000679.1:g.64224377G>A	GRCh37
NC_000017.9:g.61654839G>A	NCBI36
NG_012045.1:g.6180C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205948.11:c.65-63C>T MANE Select	ENSP00000205948.6:n.65-63C>T
ENST00000205948.10:c.65-63C>T	ENSP00000205948.6:n.65-63C>T
ENST00000577982.1:c.65-63C>T	ENSP00000464301.1:n.65-63C>T
ENST00000581797.5:c.-116-63C>T	ENSP00000463553.1:n.-116-63C>T
NM_000042.2:c.65-63C>T	NP_000033.2:n.65-63C>T
NM_000042.3:c.65-63C>T MANE Select	NP_000033.2:n.65-63C>T