Canonical Allele Identifier: CA118160603
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs10462070

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305647A>G , CM000667.2:g.44305647A>G GRCh38
NC_000005.9:g.44305749A>G , CM000667.1:g.44305749A>G GRCh37
NC_000005.8:g.44341506A>G NCBI36
NG_011446.1:g.88036T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-455T>C MANE Select ENSP00000264664.4:n.430-455T>C
ENST00000264664.4:c.430-455T>C ENSP00000264664.4:n.430-455T>C
NM_004465.1:n.430-455T>C NP_004456.1:n.430-455T>C
XM_005248264.2:c.430-455T>C XP_005248321.1:n.430-455T>C
XM_005248264.4:c.430-455T>C XP_005248321.1:n.430-455T>C
NM_004465.2:c.430-455T>C MANE Select NP_004456.1:n.430-455T>C