Canonical Allele Identifier: CA1075634120
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v3: 5-44365348-T-G
gnomAD v4: 5-44365348-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44365348T>G , CM000667.2:g.44365348T>G GRCh38
NC_000005.9:g.44365450T>G , CM000667.1:g.44365450T>G GRCh37
NC_000005.8:g.44401207T>G NCBI36
NG_011446.1:g.28335A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+23010A>C MANE Select ENSP00000264664.4:n.325+23010A>C
ENST00000264664.4:c.325+23010A>C ENSP00000264664.4:n.325+23010A>C
NM_004465.1:c.325+23010A>C NP_004456.1:n.325+23010A>C
XM_005248264.2:c.325+23010A>C XP_005248321.1:n.325+23010A>C
XM_005248264.4:c.325+23010A>C XP_005248321.1:n.325+23010A>C
NM_004465.2:c.325+23010A>C MANE Select NP_004456.1:n.325+23010A>C