Canonical Allele Identifier: CA359697870
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740047559
COSMIC: COSM1068455
MyVariant Identifiers: chr5:g.44305272T>G (hg19) chr5:g.44305170T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305170T>G , CM000667.2:g.44305170T>G GRCh38
NC_000005.9:g.44305272T>G , CM000667.1:g.44305272T>G GRCh37
NC_000005.8:g.44341029T>G NCBI36
NG_011446.1:g.88513A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.452A>C MANE Select ENSP00000264664.4:p.Lys151Thr
ENST00000264664.4:c.452A>C ENSP00000264664.4:p.Lys151Thr
NM_004465.1:c.452A>C NP_004456.1:p.Lys151Thr
XM_005248264.2:c.452A>C XP_005248321.1:p.Lys151Thr
XM_005248264.4:c.452A>C XP_005248321.1:p.Lys151Thr
NM_004465.2:c.452A>C MANE Select NP_004456.1:p.Lys151Thr
Search 100 bp 5'
Search 100 bp 3'