Canonical Allele Identifier: CA10633988
Gene: FGF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 311411
ClinVar RCV Id: RCV000290566
dbSNP Id: rs886050042
gnomAD v2: 13-22245709-AT-A
gnomAD v3: 13-21671570-AT-A
gnomAD v4: 13-21671570-AT-A
MyVariant Identifiers: chr13:g.22245717del (hg19) chr13:g.22245710del (hg19) chr13:g.21671578del (hg38) chr13:g.21671571del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.21671578del , CM000675.2:g.21671578del GRCh38
NC_000013.10:g.22245717del , CM000675.1:g.22245717del GRCh37
NC_000013.9:g.21143717del NCBI36
NG_016272.1:g.5503del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382353.6:c.-335del MANE Select ENSP00000371790.5:n.-335del
ENST00000382353.5:c.-335del ENSP00000371790.5:n.-335del
NM_002010.2:c.-335del NP_002001.1:n.-335del
NM_002010.3:c.-335del MANE Select NP_002001.1:n.-335del
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