Canonical Allele Identifier: CA2639419267
Gene: APOH HGNC NCBI

Linked Data

gnomAD v4: 17-66227938-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227938G>T , CM000679.2:g.66227938G>T GRCh38
NC_000017.10:g.64224056G>T , CM000679.1:g.64224056G>T GRCh37
NC_000017.9:g.61654518G>T NCBI36
NG_012045.1:g.6501C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+82C>A MANE Select ENSP00000205948.6:n.241+82C>A
ENST00000205948.10:c.241+82C>A ENSP00000205948.6:n.241+82C>A
ENST00000577982.1:c.241+82C>A ENSP00000464301.1:n.241+82C>A
ENST00000581797.5:c.61+82C>A ENSP00000463553.1:n.61+82C>A
NM_000042.2:c.241+82C>A NP_000033.2:n.241+82C>A
NM_000042.3:c.241+82C>A MANE Select NP_000033.2:n.241+82C>A
Search 100 bp 5'
Search 100 bp 3'