Canonical Allele Identifier: CA774239055
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1413586593
gnomAD v3: 17-66239630-C-G
gnomAD v4: 17-66239630-C-G
MyVariant Identifiers: chr17:g.64235748C>G (hg19) chr17:g.66239630C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239630C>G , CM000679.2:g.66239630C>G GRCh38
NC_000017.10:g.64235748C>G , CM000679.1:g.64235748C>G GRCh37
NC_000017.9:g.61666210C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10208G>C ENSP00000464301.1:n.-43-10208G>C
Search 100 bp 5'
Search 100 bp 3'