Canonical Allele Identifier: CA595202905

Gene: FGF8

Linked Data

• dbSNP Id: rs372721795
• gnomAD v2: 10-103534451-C-G
• gnomAD v4: 10-101774694-C-G
• MyVariant Identifiers: chr10:g.103534451C>G (hg19) ; chr10:g.101774694C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774694C>G , CM000672.2:g.101774694C>G	GRCh38
NC_000010.10:g.103534451C>G , CM000672.1:g.103534451C>G	GRCh37
NC_000010.9:g.103524441C>G	NCBI36
NG_007151.1:g.6377G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.337+38G>C MANE Select	ENSP00000321797.2:n.337+38G>C
ENST00000618991.5:c.25+38G>C	ENSP00000484420.1:n.25+38G>C
ENST00000344255.8:c.304+38G>C	ENSP00000340039.3:n.304+38G>C
ENST00000320185.6:c.337+38G>C	ENSP00000321797.2:n.337+38G>C
ENST00000344255.7:c.304+38G>C	ENSP00000340039.3:n.304+38G>C
ENST00000346714.7:c.217+38G>C	ENSP00000344306.3:n.217+38G>C
ENST00000347978.2:c.250+38G>C	ENSP00000321945.2:n.250+38G>C
ENST00000469792.6:c.*301+38G>C	ENSP00000473299.1:n.*301+38G>C
ENST00000485728.1:n.213+38G>C
ENST00000618991.4:c.25+38G>C	ENSP00000484420.1:n.25+38G>C
NM_001206389.1:c.25+38G>C	NP_001193318.1:n.25+38G>C
NM_006119.4:c.250+38G>C	NP_006110.1:n.250+38G>C
NM_033163.3:c.337+38G>C	NP_149353.1:n.337+38G>C
NM_033164.3:c.304+38G>C	NP_149354.1:n.304+38G>C
NM_033165.3:c.217+38G>C	NP_149355.1:n.217+38G>C
XM_011539509.1:c.259+38G>C	XP_011537811.1:n.259+38G>C
NM_006119.5:c.250+38G>C	NP_006110.1:n.250+38G>C
NM_033163.4:c.337+38G>C	NP_149353.1:n.337+38G>C
NM_033164.4:c.304+38G>C	NP_149354.1:n.304+38G>C
NM_033165.4:c.217+38G>C	NP_149355.1:n.217+38G>C
NM_001206389.2:c.25+38G>C	NP_001193318.1:n.25+38G>C
NM_006119.6:c.250+38G>C	NP_006110.1:n.250+38G>C
NM_033163.5:c.337+38G>C MANE Select	NP_149353.1:n.337+38G>C
NM_033165.5:c.217+38G>C	NP_149355.1:n.217+38G>C