Canonical Allele Identifier: CA172903342
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs895829282
MyVariant Identifiers: chr8:g.16850040C>A (hg19) chr8:g.16992531C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992531C>A , CM000670.2:g.16992531C>A GRCh38
NC_000008.10:g.16850040C>A , CM000670.1:g.16850040C>A GRCh37
NC_000008.9:g.16894411C>A NCBI36
NG_015978.1:g.14635G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*541G>T MANE Select ENSP00000180166.5:n.*541G>T
ENST00000180166.5:c.*541G>T ENSP00000180166.5:n.*541G>T
NM_019851.3:c.*541G>T MANE Select NP_062825.1:n.*541G>T
Search 100 bp 5'
Search 100 bp 3'