Canonical Allele Identifier: CA649973566
Gene: FGF10 HGNC NCBI

Linked Data

COSMIC: COSN2107406
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44388282C>G , CM000667.2:g.44388282C>G GRCh38
NC_000005.9:g.44388384C>G , CM000667.1:g.44388384C>G GRCh37
NC_000005.8:g.44424141C>G NCBI36
NG_011446.1:g.5401G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264664.5:c.325+76G>C MANE Select ENSP00000264664.4:n.325+76G>C
ENST00000264664.4:c.325+76G>C ENSP00000264664.4:n.325+76G>C
NM_004465.1:c.325+76G>C NP_004456.1:n.325+76G>C
XM_005248264.2:c.325+76G>C XP_005248321.1:n.325+76G>C
XM_005248264.4:c.325+76G>C XP_005248321.1:n.325+76G>C
NM_004465.2:c.325+76G>C MANE Select NP_004456.1:n.325+76G>C
Search 100 bp 5'
Search 100 bp 3'