Canonical Allele Identifier: CA172903571
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs1024379139
gnomAD v2: 8-16850286-C-A
gnomAD v3: 8-16992777-C-A
gnomAD v4: 8-16992777-C-A
MyVariant Identifiers: chr8:g.16850286C>A (hg19) chr8:g.16992777C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992777C>A , CM000670.2:g.16992777C>A GRCh38
NC_000008.10:g.16850286C>A , CM000670.1:g.16850286C>A GRCh37
NC_000008.9:g.16894657C>A NCBI36
NG_015978.1:g.14389G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*295G>T MANE Select ENSP00000180166.5:n.*295G>T
ENST00000180166.5:c.*295G>T ENSP00000180166.5:n.*295G>T
NM_019851.3:c.*295G>T MANE Select NP_062825.1:n.*295G>T
Search 100 bp 5'
Search 100 bp 3'