Canonical Allele Identifier: CA2686252312
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16992791-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992791C>T , CM000670.2:g.16992791C>T GRCh38
NC_000008.10:g.16850300C>T , CM000670.1:g.16850300C>T GRCh37
NC_000008.9:g.16894671C>T NCBI36
NG_015978.1:g.14375G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*281G>A MANE Select ENSP00000180166.5:n.*281G>A
ENST00000180166.5:c.*281G>A ENSP00000180166.5:n.*281G>A
NM_019851.3:c.*281G>A MANE Select NP_062825.1:n.*281G>A
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