Canonical Allele Identifier: CA2673772858
Gene: FGF10 HGNC NCBI

Linked Data

gnomAD v4: 5-44388264-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388264A>G , CM000667.2:g.44388264A>G GRCh38
NC_000005.9:g.44388366A>G , CM000667.1:g.44388366A>G GRCh37
NC_000005.8:g.44424123A>G NCBI36
NG_011446.1:g.5419T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.325+94T>C MANE Select ENSP00000264664.4:n.325+94T>C
ENST00000264664.4:c.325+94T>C ENSP00000264664.4:n.325+94T>C
NM_004465.1:c.325+94T>C NP_004456.1:n.325+94T>C
XM_005248264.2:c.325+94T>C XP_005248321.1:n.325+94T>C
XM_005248264.4:c.325+94T>C XP_005248321.1:n.325+94T>C
NM_004465.2:c.325+94T>C MANE Select NP_004456.1:n.325+94T>C
Search 100 bp 5'
Search 100 bp 3'