Canonical Allele Identifier: CA370394469
Gene: FGF20 HGNC NCBI

Linked Data

gnomAD v4: 8-16993226-G-C
MyVariant Identifiers: chr8:g.16850735G>C (hg19) chr8:g.16993226G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993226G>C , CM000670.2:g.16993226G>C GRCh38
NC_000008.10:g.16850735G>C , CM000670.1:g.16850735G>C GRCh37
NC_000008.9:g.16895106G>C NCBI36
NG_015978.1:g.13940C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.482C>G MANE Select ENSP00000180166.5:p.Thr161Ser
ENST00000180166.5:c.482C>G ENSP00000180166.5:p.Thr161Ser
ENST00000519941.1:c.186C>G
NM_019851.2:c.482C>G NP_062825.1:p.Thr161Ser
NM_019851.3:c.482C>G MANE Select NP_062825.1:p.Thr161Ser
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