Canonical Allele Identifier: CA400683744

Gene: APOH

Linked Data

• COSMIC: COSM132660
• MyVariant Identifiers: chr17:g.64224180G>A (hg19) ; chr17:g.66228062G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.66228062G>A , CM000679.2:g.66228062G>A	GRCh38
NC_000017.10:g.64224180G>A , CM000679.1:g.64224180G>A	GRCh37
NC_000017.9:g.61654642G>A	NCBI36
NG_012045.1:g.6377C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205948.11:c.199C>T MANE Select	ENSP00000205948.6:p.Pro67Ser
ENST00000205948.10:c.199C>T	ENSP00000205948.6:p.Pro67Ser
ENST00000577982.1:c.199C>T	ENSP00000464301.1:p.Pro67Ser
ENST00000581797.5:c.19C>T	ENSP00000463553.1:p.Pro7Ser
NM_000042.2:c.199C>T	NP_000033.2:p.Pro67Ser
NM_000042.3:c.199C>T MANE Select	NP_000033.2:p.Pro67Ser