Canonical Allele Identifier: CA1093201884

Gene: FYN

Linked Data

• dbSNP Id: rs1774341682
• gnomAD v3: 6-111873249-A-G
• gnomAD v4: 6-111873249-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873249A>G , CM000668.2:g.111873249A>G	GRCh38
NC_000006.11:g.112194452A>G , CM000668.1:g.112194452A>G	GRCh37
NC_000006.10:g.112301145A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-404T>C	ENSP00000357671.3:n.-404T>C
ENST00000354650.7:c.-404T>C MANE Select	ENSP00000346671.3:n.-404T>C
ENST00000368678.8:c.-334T>C	ENSP00000357667.4:n.-334T>C
ENST00000484067.6:c.-361+21T>C	ENSP00000428983.1:n.-361+21T>C
ENST00000518295.5:c.-521T>C	ENSP00000428695.1:n.-521T>C
ENST00000523238.5:c.-363T>C	ENSP00000430364.1:n.-363T>C
NM_002037.5:c.-404T>C MANE Select	NP_002028.1:n.-404T>C
XM_005266890.2:c.-404T>C	XP_005266947.1:n.-404T>C
XM_005266892.2:c.-404T>C	XP_005266949.1:n.-404T>C
XM_011535662.1:c.-404T>C	XP_011533964.1:n.-404T>C
XM_011535663.1:c.-363T>C	XP_011533965.1:n.-363T>C
XM_011536304.1:c.518A>G	XP_011534606.1:p.Asp173Gly
XM_024446614.1:c.518A>G	XP_024302382.1:p.Asp173Gly