Canonical Allele Identifier: CA293118537
Gene: APOH HGNC NCBI

Linked Data

dbSNP Id: rs113836465
gnomAD v4: 17-66228197-C-T
MyVariant Identifiers: chr17:g.64224315C>T (hg19) chr17:g.66228197C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66228197C>T , CM000679.2:g.66228197C>T GRCh38
NC_000017.10:g.64224315C>T , CM000679.1:g.64224315C>T GRCh37
NC_000017.9:g.61654777C>T NCBI36
NG_012045.1:g.6242G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205948.11:c.65-1G>A MANE Select ENSP00000205948.6:n.65-1G>A
ENST00000205948.10:c.65-1G>A ENSP00000205948.6:n.65-1G>A
ENST00000577982.1:c.65-1G>A ENSP00000464301.1:n.65-1G>A
ENST00000581797.5:c.-116-1G>A ENSP00000463553.1:n.-116-1G>A
NM_000042.2:c.65-1G>A NP_000033.2:n.65-1G>A
NM_000042.3:c.65-1G>A MANE Select NP_000033.2:n.65-1G>A
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