Canonical Allele Identifier: CA2568056344
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v4: 5-44388297-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388297C>A , CM000667.2:g.44388297C>A GRCh38
NC_000005.9:g.44388399C>A , CM000667.1:g.44388399C>A GRCh37
NC_000005.8:g.44424156C>A NCBI36
NG_011446.1:g.5386G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+61G>T MANE Select ENSP00000264664.4:n.325+61G>T
ENST00000264664.4:c.325+61G>T ENSP00000264664.4:n.325+61G>T
NM_004465.1:c.325+61G>T NP_004456.1:n.325+61G>T
XM_005248264.2:c.325+61G>T XP_005248321.1:n.325+61G>T
XM_005248264.4:c.325+61G>T XP_005248321.1:n.325+61G>T
NM_004465.2:c.325+61G>T MANE Select NP_004456.1:n.325+61G>T