Canonical Allele Identifier: CA118166984
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs12517396
gnomAD v2: 5-44359526-C-A
gnomAD v3: 5-44359424-C-A
gnomAD v4: 5-44359424-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44359424C>A , CM000667.2:g.44359424C>A GRCh38
NC_000005.9:g.44359526C>A , CM000667.1:g.44359526C>A GRCh37
NC_000005.8:g.44395283C>A NCBI36
NG_011446.1:g.34259G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+28934G>T MANE Select ENSP00000264664.4:n.325+28934G>T
ENST00000264664.4:c.325+28934G>T ENSP00000264664.4:n.325+28934G>T
NM_004465.1:c.325+28934G>T NP_004456.1:n.325+28934G>T
XM_005248264.2:c.325+28934G>T XP_005248321.1:n.325+28934G>T
XM_005248264.4:c.325+28934G>T XP_005248321.1:n.325+28934G>T
NM_004465.2:c.325+28934G>T MANE Select NP_004456.1:n.325+28934G>T