Canonical Allele Identifier: CA2686252396
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992895-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992895A>G , CM000670.2:g.16992895A>G GRCh38
NC_000008.10:g.16850404A>G , CM000670.1:g.16850404A>G GRCh37
NC_000008.9:g.16894775A>G NCBI36
NG_015978.1:g.14271T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*177T>C MANE Select ENSP00000180166.5:n.*177T>C
ENST00000180166.5:c.*177T>C ENSP00000180166.5:n.*177T>C
NM_019851.2:c.*177T>C NP_062825.1:n.*177T>C
NM_019851.3:c.*177T>C MANE Select NP_062825.1:n.*177T>C
Search 100 bp 5'
Search 100 bp 3'