Canonical Allele Identifier: CA459633835
Gene: FGF20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.16850626T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993117T>C , CM000670.2:g.16993117T>C GRCh38
NC_000008.10:g.16850626T>C , CM000670.1:g.16850626T>C GRCh37
NC_000008.9:g.16894997T>C NCBI36
NG_015978.1:g.14049A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.591A>G MANE Select ENSP00000180166.5:p.Pro197=
ENST00000180166.5:c.591A>G ENSP00000180166.5:p.Pro197=
ENST00000519941.1:c.295A>G
NM_019851.2:c.591A>G NP_062825.1:p.Pro197=
NM_019851.3:c.591A>G MANE Select NP_062825.1:p.Pro197=
Search 100 bp 5'
Search 100 bp 3'