Canonical Allele Identifier: CA3258539
Gene: FGF10 HGNC NCBI

Linked Data

dbSNP Id: rs370941301
gnomAD v2: 5-44388461-G-A
gnomAD v4: 5-44388359-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388359G>A , CM000667.2:g.44388359G>A GRCh38
NC_000005.9:g.44388461G>A , CM000667.1:g.44388461G>A GRCh37
NC_000005.8:g.44424218G>A NCBI36
NG_011446.1:g.5324C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264664.5:c.324C>T MANE Select ENSP00000264664.4:p.Tyr108=
ENST00000264664.4:c.324C>T ENSP00000264664.4:p.Tyr108=
NM_004465.1:c.324C>T NP_004456.1:p.Tyr108=
XM_005248264.2:c.324C>T XP_005248321.1:p.Tyr108=
XM_005248264.4:c.324C>T XP_005248321.1:p.Tyr108=
NM_004465.2:c.324C>T MANE Select NP_004456.1:p.Tyr108=