Canonical Allele Identifier: CA293120694
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs1020200486
MyVariant Identifiers: chr17:g.64236027T>C (hg19) chr17:g.66239909T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66239909T>C , CM000679.2:g.66239909T>C GRCh38
NC_000017.10:g.64236027T>C , CM000679.1:g.64236027T>C GRCh37
NC_000017.9:g.61666489T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577982.1:c.-43-10487A>G ENSP00000464301.1:n.-43-10487A>G
Search 100 bp 5'
Search 100 bp 3'