Canonical Allele Identifier: CA817295382

Gene: FYN

Linked Data

• dbSNP Id: rs1422136505
• gnomAD v3: 6-111873238-G-A
• gnomAD v4: 6-111873238-G-A
• MyVariant Identifiers: chr6:g.112194441G>A (hg19) ; chr6:g.111873238G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873238G>A , CM000668.2:g.111873238G>A	GRCh38
NC_000006.11:g.112194441G>A , CM000668.1:g.112194441G>A	GRCh37
NC_000006.10:g.112301134G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-393C>T	ENSP00000357671.3:n.-393C>T
ENST00000354650.7:c.-393C>T MANE Select	ENSP00000346671.3:n.-393C>T
ENST00000368678.8:c.-323C>T	ENSP00000357667.4:n.-323C>T
ENST00000484067.6:c.-360-33C>T	ENSP00000428983.1:n.-360-33C>T
ENST00000518295.5:c.-510C>T	ENSP00000428695.1:n.-510C>T
ENST00000523238.5:c.-352C>T	ENSP00000430364.1:n.-352C>T
NM_002037.5:c.-393C>T MANE Select	NP_002028.1:n.-393C>T
XM_005266890.2:c.-393C>T	XP_005266947.1:n.-393C>T
XM_005266892.2:c.-393C>T	XP_005266949.1:n.-393C>T
XM_011535662.1:c.-393C>T	XP_011533964.1:n.-393C>T
XM_011535663.1:c.-352C>T	XP_011533965.1:n.-352C>T
XM_011536304.1:c.507G>A	XP_011534606.1:p.Arg169=
XM_024446614.1:c.507G>A	XP_024302382.1:p.Arg169=