Canonical Allele Identifier: CA2686252421
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992910-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992910T>C , CM000670.2:g.16992910T>C GRCh38
NC_000008.10:g.16850419T>C , CM000670.1:g.16850419T>C GRCh37
NC_000008.9:g.16894790T>C NCBI36
NG_015978.1:g.14256A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*162A>G MANE Select ENSP00000180166.5:n.*162A>G
ENST00000180166.5:c.*162A>G ENSP00000180166.5:n.*162A>G
NM_019851.2:c.*162A>G NP_062825.1:n.*162A>G
NM_019851.3:c.*162A>G MANE Select NP_062825.1:n.*162A>G
Search 100 bp 5'
Search 100 bp 3'