Canonical Allele Identifier: CA10643016
Gene: FGF9 HGNC NCBI

Linked Data

ClinVar Variation Id: 311416
ClinVar RCV Id: RCV000398437
dbSNP Id: rs10624265
gnomAD v2: 13-22245927-C-CTT
gnomAD v3: 13-21671788-C-CTT
gnomAD v4: 13-21671788-C-CTT
COSMIC: COSN20110424 COSN20110425 COSN20110426 COSN20110427
MyVariant Identifiers: chr13:g.22245934_22245935dupTT (hg19) chr13:g.22245935_22245936insTT (hg19) chr13:g.22245927_22245928insTT (hg19) chr13:g.21671795_21671796dupTT (hg38) chr13:g.21671796_21671797insTT (hg38) chr13:g.21671788_21671789insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.21671795_21671796dup , CM000675.2:g.21671795_21671796dup GRCh38
NC_000013.10:g.22245934_22245935dup , CM000675.1:g.22245934_22245935dup GRCh37
NC_000013.9:g.21143934_21143935dup NCBI36
NG_016272.1:g.5720_5721dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382353.6:c.-118_-117dup MANE Select ENSP00000371790.5:n.-118_-117dup
ENST00000382353.5:c.-118_-117dup ENSP00000371790.5:n.-118_-117dup
NM_002010.2:c.-118_-117dup NP_002001.1:n.-118_-117dup
NM_002010.3:c.-118_-117dup MANE Select NP_002001.1:n.-118_-117dup
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