Canonical Allele Identifier: CA558944630

Gene: FGF10

Linked Data

• dbSNP Id: rs1240169032
• gnomAD v2: 5-44359585-T-C
• gnomAD v3: 5-44359483-T-C
• gnomAD v4: 5-44359483-T-C
• MyVariant Identifiers: chr5:g.44359585T>C (hg19) ; chr5:g.44359483T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.44359483T>C , CM000667.2:g.44359483T>C	GRCh38
NC_000005.9:g.44359585T>C , CM000667.1:g.44359585T>C	GRCh37
NC_000005.8:g.44395342T>C	NCBI36
NG_011446.1:g.34200A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264664.5:c.325+28875A>G MANE Select	ENSP00000264664.4:n.325+28875A>G
ENST00000264664.4:c.325+28875A>G	ENSP00000264664.4:n.325+28875A>G
NM_004465.1:c.325+28875A>G	NP_004456.1:n.325+28875A>G
XM_005248264.2:c.325+28875A>G	XP_005248321.1:n.325+28875A>G
XM_005248264.4:c.325+28875A>G	XP_005248321.1:n.325+28875A>G
NM_004465.2:c.325+28875A>G MANE Select	NP_004456.1:n.325+28875A>G