Canonical Allele Identifier: CA1093201810

Gene: FYN

Linked Data

• dbSNP Id: rs1774338690
• gnomAD v3: 6-111873132-A-C
• gnomAD v4: 6-111873132-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873132A>C , CM000668.2:g.111873132A>C	GRCh38
NC_000006.11:g.112194335A>C , CM000668.1:g.112194335A>C	GRCh37
NC_000006.10:g.112301028A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-287T>G	ENSP00000357671.3:n.-287T>G
ENST00000354650.7:c.-287T>G MANE Select	ENSP00000346671.3:n.-287T>G
ENST00000368678.8:c.-217T>G	ENSP00000357667.4:n.-217T>G
ENST00000484067.6:c.-287T>G	ENSP00000428983.1:n.-287T>G
ENST00000518295.5:c.-404T>G	ENSP00000428695.1:n.-404T>G
ENST00000523238.5:c.-246T>G	ENSP00000430364.1:n.-246T>G
NM_002037.5:c.-287T>G MANE Select	NP_002028.1:n.-287T>G
XM_005266890.2:c.-287T>G	XP_005266947.1:n.-287T>G
XM_005266892.2:c.-287T>G	XP_005266949.1:n.-287T>G
XM_011535662.1:c.-287T>G	XP_011533964.1:n.-287T>G
XM_011535663.1:c.-246T>G	XP_011533965.1:n.-246T>G
XM_011536304.1:c.401A>C	XP_011534606.1:p.Asn134Thr
XM_024446614.1:c.401A>C	XP_024302382.1:p.Asn134Thr