Canonical Allele Identifier: CA1543124701
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs1741423490

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359353A>T , CM000667.2:g.44359353A>T GRCh38
NC_000005.9:g.44359455A>T , CM000667.1:g.44359455A>T GRCh37
NC_000005.8:g.44395212A>T NCBI36
NG_011446.1:g.34330T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+29005T>A MANE Select ENSP00000264664.4:n.325+29005T>A
ENST00000264664.4:c.325+29005T>A ENSP00000264664.4:n.325+29005T>A
NM_004465.1:c.325+29005T>A NP_004456.1:n.325+29005T>A
XM_005248264.2:c.325+29005T>A XP_005248321.1:n.325+29005T>A
XM_005248264.4:c.325+29005T>A XP_005248321.1:n.325+29005T>A
NM_004465.2:c.325+29005T>A MANE Select NP_004456.1:n.325+29005T>A