Canonical Allele Identifier: CA2607896334

Gene: FYN

Linked Data

• dbSNP Id: rs2114263897
• gnomAD v4: 6-111873081-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873081T>C , CM000668.2:g.111873081T>C	GRCh38
NC_000006.11:g.112194284T>C , CM000668.1:g.112194284T>C	GRCh37
NC_000006.10:g.112300977T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-236A>G	ENSP00000357671.3:n.-236A>G
ENST00000354650.7:c.-236A>G MANE Select	ENSP00000346671.3:n.-236A>G
ENST00000368678.8:c.-166A>G	ENSP00000357667.4:n.-166A>G
ENST00000484067.6:c.-236A>G	ENSP00000428983.1:n.-236A>G
ENST00000518295.5:c.-353A>G	ENSP00000428695.1:n.-353A>G
ENST00000523238.5:c.-195A>G	ENSP00000430364.1:n.-195A>G
NM_002037.5:c.-236A>G MANE Select	NP_002028.1:n.-236A>G
XM_005266890.2:c.-236A>G	XP_005266947.1:n.-236A>G
XM_005266892.2:c.-236A>G	XP_005266949.1:n.-236A>G
XM_011535662.1:c.-236A>G	XP_011533964.1:n.-236A>G
XM_011535663.1:c.-195A>G	XP_011533965.1:n.-195A>G
XM_011536304.1:c.350T>C	XP_011534606.1:p.Phe117Ser
XM_024446614.1:c.350T>C	XP_024302382.1:p.Phe117Ser