Canonical Allele Identifier: CA810998012

Gene: FGF10

Linked Data

• dbSNP Id: rs1278243986
• MyVariant Identifiers: chr5:g.44359438G>A (hg19) ; chr5:g.44359336G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44359336G>A , CM000667.2:g.44359336G>A	GRCh38
NC_000005.9:g.44359438G>A , CM000667.1:g.44359438G>A	GRCh37
NC_000005.8:g.44395195G>A	NCBI36
NG_011446.1:g.34347C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.325+29022C>T MANE Select	ENSP00000264664.4:n.325+29022C>T
ENST00000264664.4:c.325+29022C>T	ENSP00000264664.4:n.325+29022C>T
NM_004465.1:c.325+29022C>T	NP_004456.1:n.325+29022C>T
XM_005248264.2:c.325+29022C>T	XP_005248321.1:n.325+29022C>T
XM_005248264.4:c.325+29022C>T	XP_005248321.1:n.325+29022C>T
NM_004465.2:c.325+29022C>T MANE Select	NP_004456.1:n.325+29022C>T