Canonical Allele Identifier: CA1767395477
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809939243
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992591A>G , CM000670.2:g.16992591A>G GRCh38
NC_000008.10:g.16850100A>G , CM000670.1:g.16850100A>G GRCh37
NC_000008.9:g.16894471A>G NCBI36
NG_015978.1:g.14575T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*481T>C MANE Select ENSP00000180166.5:n.*481T>C
ENST00000180166.5:c.*481T>C ENSP00000180166.5:n.*481T>C
NM_019851.3:c.*481T>C MANE Select NP_062825.1:n.*481T>C
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