Canonical Allele Identifier: CA626911835
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs545764645
gnomAD v2: 17-64224017-A-C
gnomAD v3: 17-66227899-A-C
gnomAD v4: 17-66227899-A-C
MyVariant Identifiers: chr17:g.64224017A>C (hg19) chr17:g.66227899A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66227899A>C , CM000679.2:g.66227899A>C GRCh38
NC_000017.10:g.64224017A>C , CM000679.1:g.64224017A>C GRCh37
NC_000017.9:g.61654479A>C NCBI36
NG_012045.1:g.6540T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.241+121T>G MANE Select ENSP00000205948.6:n.241+121T>G
ENST00000205948.10:c.241+121T>G ENSP00000205948.6:n.241+121T>G
ENST00000577982.1:c.241+121T>G ENSP00000464301.1:n.241+121T>G
ENST00000581797.5:c.61+121T>G ENSP00000463553.1:n.61+121T>G
NM_000042.2:c.241+121T>G NP_000033.2:n.241+121T>G
NM_000042.3:c.241+121T>G MANE Select NP_000033.2:n.241+121T>G
Search 100 bp 5'
Search 100 bp 3'