Canonical Allele Identifier: CA1767395688
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1809945831

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992839A>C , CM000670.2:g.16992839A>C GRCh38
NC_000008.10:g.16850348A>C , CM000670.1:g.16850348A>C GRCh37
NC_000008.9:g.16894719A>C NCBI36
NG_015978.1:g.14327T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*233T>G MANE Select ENSP00000180166.5:n.*233T>G
ENST00000180166.5:c.*233T>G ENSP00000180166.5:n.*233T>G
NM_019851.2:c.*233T>G NP_062825.1:n.*233T>G
NM_019851.3:c.*233T>G MANE Select NP_062825.1:n.*233T>G