Canonical Allele Identifier: CA370394302
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809955148
MyVariant Identifiers: chr8:g.16850652G>C (hg19) chr8:g.16993143G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993143G>C , CM000670.2:g.16993143G>C GRCh38
NC_000008.10:g.16850652G>C , CM000670.1:g.16850652G>C GRCh37
NC_000008.9:g.16895023G>C NCBI36
NG_015978.1:g.14023C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.565C>G MANE Select ENSP00000180166.5:p.His189Asp
ENST00000180166.5:c.565C>G ENSP00000180166.5:p.His189Asp
ENST00000519941.1:c.269C>G
NM_019851.2:c.565C>G NP_062825.1:p.His189Asp
NM_019851.3:c.565C>G MANE Select NP_062825.1:p.His189Asp
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