Canonical Allele Identifier: CA172904188
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1051138244
MyVariant Identifiers: chr8:g.16850697T>C (hg19) chr8:g.16993188T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993188T>C , CM000670.2:g.16993188T>C GRCh38
NC_000008.10:g.16850697T>C , CM000670.1:g.16850697T>C GRCh37
NC_000008.9:g.16895068T>C NCBI36
NG_015978.1:g.13978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.520A>G MANE Select ENSP00000180166.5:p.Thr174Ala
ENST00000180166.5:c.520A>G ENSP00000180166.5:p.Thr174Ala
ENST00000519941.1:c.224A>G
NM_019851.2:c.520A>G NP_062825.1:p.Thr174Ala
NM_019851.3:c.520A>G MANE Select NP_062825.1:p.Thr174Ala
Search 100 bp 5'
Search 100 bp 3'