Canonical Allele Identifier: CA1075634124
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v3: 5-44365349-G-C
gnomAD v4: 5-44365349-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365349G>C , CM000667.2:g.44365349G>C GRCh38
NC_000005.9:g.44365451G>C , CM000667.1:g.44365451G>C GRCh37
NC_000005.8:g.44401208G>C NCBI36
NG_011446.1:g.28334C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23009C>G MANE Select ENSP00000264664.4:n.325+23009C>G
ENST00000264664.4:c.325+23009C>G ENSP00000264664.4:n.325+23009C>G
NM_004465.1:c.325+23009C>G NP_004456.1:n.325+23009C>G
XM_005248264.2:c.325+23009C>G XP_005248321.1:n.325+23009C>G
XM_005248264.4:c.325+23009C>G XP_005248321.1:n.325+23009C>G
NM_004465.2:c.325+23009C>G MANE Select NP_004456.1:n.325+23009C>G