Canonical Allele Identifier: CA817295315

Gene: FYN

Linked Data

• dbSNP Id: rs1310776029
• gnomAD v3: 6-111873136-C-T
• gnomAD v4: 6-111873136-C-T
• MyVariant Identifiers: chr6:g.112194339C>T (hg19) ; chr6:g.111873136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873136C>T , CM000668.2:g.111873136C>T	GRCh38
NC_000006.11:g.112194339C>T , CM000668.1:g.112194339C>T	GRCh37
NC_000006.10:g.112301032C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-291G>A	ENSP00000357671.3:n.-291G>A
ENST00000354650.7:c.-291G>A MANE Select	ENSP00000346671.3:n.-291G>A
ENST00000368678.8:c.-221G>A	ENSP00000357667.4:n.-221G>A
ENST00000484067.6:c.-291G>A	ENSP00000428983.1:n.-291G>A
ENST00000518295.5:c.-408G>A	ENSP00000428695.1:n.-408G>A
ENST00000523238.5:c.-250G>A	ENSP00000430364.1:n.-250G>A
NM_002037.5:c.-291G>A MANE Select	NP_002028.1:n.-291G>A
XM_005266890.2:c.-291G>A	XP_005266947.1:n.-291G>A
XM_005266892.2:c.-291G>A	XP_005266949.1:n.-291G>A
XM_011535662.1:c.-291G>A	XP_011533964.1:n.-291G>A
XM_011535663.1:c.-250G>A	XP_011533965.1:n.-250G>A
XM_011536304.1:c.405C>T	XP_011534606.1:p.Pro135=
XM_024446614.1:c.405C>T	XP_024302382.1:p.Pro135=