Canonical Allele Identifier: CA526677640
Gene: CFAP45 HGNC NCBI

Linked Data

dbSNP Id: rs1454839925
gnomAD v2: 1-159856563-G-T
gnomAD v3: 1-159886773-G-T
gnomAD v4: 1-159886773-G-T
MyVariant Identifiers: chr1:g.159856563G>T (hg19) chr1:g.159886773G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886773G>T , CM000663.2:g.159886773G>T GRCh38
NC_000001.10:g.159856563G>T , CM000663.1:g.159856563G>T GRCh37
NC_000001.9:g.158123187G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.589-84C>A MANE Select ENSP00000357079.4:n.589-84C>A
ENST00000368099.8:c.589-84C>A ENSP00000357079.4:n.589-84C>A
ENST00000426543.6:c.334-84C>A ENSP00000403044.2:n.334-84C>A
ENST00000476696.5:c.589-84C>A ENSP00000483972.1:n.589-84C>A
ENST00000479940.2:c.334-84C>A ENSP00000478944.1:n.334-84C>A
NM_012337.2:c.589-84C>A NP_036469.2:n.589-84C>A
NM_012337.3:c.589-84C>A MANE Select NP_036469.2:n.589-84C>A
Search 100 bp 5'
Search 100 bp 3'