Canonical Allele Identifier: CA1543080293
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1740056930
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44305574C>T , CM000667.2:g.44305574C>T GRCh38
NC_000005.9:g.44305676C>T , CM000667.1:g.44305676C>T GRCh37
NC_000005.8:g.44341433C>T NCBI36
NG_011446.1:g.88109G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.430-382G>A MANE Select ENSP00000264664.4:n.430-382G>A
ENST00000264664.4:c.430-382G>A ENSP00000264664.4:n.430-382G>A
NM_004465.1:c.430-382G>A NP_004456.1:n.430-382G>A
XM_005248264.2:c.430-382G>A XP_005248321.1:n.430-382G>A
XM_005248264.4:c.430-382G>A XP_005248321.1:n.430-382G>A
NM_004465.2:c.430-382G>A MANE Select NP_004456.1:n.430-382G>A
Search 100 bp 5'
Search 100 bp 3'