Canonical Allele Identifier: CA172903813
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs937947933
gnomAD v2: 8-16850427-G-GT
gnomAD v3: 8-16992918-G-GT
gnomAD v4: 8-16992918-G-GT
MyVariant Identifiers: chr8:g.16850427_16850428insT (hg19) chr8:g.16992918_16992919insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992926dup , CM000670.2:g.16992926dup GRCh38
NC_000008.10:g.16850435dup , CM000670.1:g.16850435dup GRCh37
NC_000008.9:g.16894806dup NCBI36
NG_015978.1:g.14247dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*153dup MANE Select ENSP00000180166.5:n.*153dup
ENST00000180166.5:c.*153dup ENSP00000180166.5:n.*153dup
NM_019851.2:c.*153dup NP_062825.1:n.*153dup
NM_019851.3:c.*153dup MANE Select NP_062825.1:n.*153dup
Search 100 bp 5'
Search 100 bp 3'