Canonical Allele Identifier: CA172903214
Gene: FGF20 HGNC NCBI

Linked Data

dbSNP Id: rs76141694
gnomAD v2: 8-16849924-G-A
gnomAD v3: 8-16992415-G-A
gnomAD v4: 8-16992415-G-A
MyVariant Identifiers: chr8:g.16849924G>A (hg19) chr8:g.16992415G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992415G>A , CM000670.2:g.16992415G>A GRCh38
NC_000008.10:g.16849924G>A , CM000670.1:g.16849924G>A GRCh37
NC_000008.9:g.16894295G>A NCBI36
NG_015978.1:g.14751C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.*657C>T MANE Select ENSP00000180166.5:n.*657C>T
ENST00000180166.5:c.*657C>T ENSP00000180166.5:n.*657C>T
NM_019851.3:c.*657C>T MANE Select NP_062825.1:n.*657C>T
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