Canonical Allele Identifier: CA359697867
Gene: FGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2542857
ClinVar RCV Id: RCV003287088
MyVariant Identifiers: chr5:g.44305271C>G (hg19) chr5:g.44305169C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305169C>G , CM000667.2:g.44305169C>G GRCh38
NC_000005.9:g.44305271C>G , CM000667.1:g.44305271C>G GRCh37
NC_000005.8:g.44341028C>G NCBI36
NG_011446.1:g.88514G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.453G>C MANE Select ENSP00000264664.4:p.Lys151Asn
ENST00000264664.4:c.453G>C ENSP00000264664.4:p.Lys151Asn
NM_004465.1:c.453G>C NP_004456.1:p.Lys151Asn
XM_005248264.2:c.453G>C XP_005248321.1:p.Lys151Asn
XM_005248264.4:c.453G>C XP_005248321.1:p.Lys151Asn
NM_004465.2:c.453G>C MANE Select NP_004456.1:p.Lys151Asn
Search 100 bp 5'
Search 100 bp 3'