Canonical Allele Identifier: CA501476209
Gene: APOH HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.64224307G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228189G>C , CM000679.2:g.66228189G>C GRCh38
NC_000017.10:g.64224307G>C , CM000679.1:g.64224307G>C GRCh37
NC_000017.9:g.61654769G>C NCBI36
NG_012045.1:g.6250C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.72C>G MANE Select ENSP00000205948.6:p.Pro24=
ENST00000205948.10:c.72C>G ENSP00000205948.6:p.Pro24=
ENST00000577982.1:c.72C>G ENSP00000464301.1:p.Pro24=
ENST00000581797.5:c.-109C>G ENSP00000463553.1:n.-109C>G
NM_000042.2:c.72C>G NP_000033.2:p.Pro24=
NM_000042.3:c.72C>G MANE Select NP_000033.2:p.Pro24=
Search 100 bp 5'
Search 100 bp 3'