Canonical Allele Identifier: CA475222151
Gene: FGF3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.69633573G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.69818805G>C , CM000673.2:g.69818805G>C GRCh38
NC_000011.9:g.69633573G>C , CM000673.1:g.69633573G>C GRCh37
NC_000011.8:g.69342510G>C NCBI36
NG_009016.1:g.5620C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000334134.4:c.129C>G MANE Select ENSP00000334122.2:p.Pro43=
ENST00000334134.2:c.129C>G ENSP00000334122.2:p.Pro43=
NM_005247.2:c.129C>G NP_005238.1:p.Pro43=
NM_005247.3:c.129C>G NP_005238.1:p.Pro43=
NM_005247.4:c.129C>G MANE Select NP_005238.1:p.Pro43=
Search 100 bp 5'
Search 100 bp 3'