Canonical Allele Identifier: CA817295384

Gene: FYN

Linked Data

• dbSNP Id: rs1252852894
• gnomAD v3: 6-111873240-C-T
• gnomAD v4: 6-111873240-C-T
• MyVariant Identifiers: chr6:g.112194443C>T (hg19) ; chr6:g.111873240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873240C>T , CM000668.2:g.111873240C>T	GRCh38
NC_000006.11:g.112194443C>T , CM000668.1:g.112194443C>T	GRCh37
NC_000006.10:g.112301136C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-395G>A	ENSP00000357671.3:n.-395G>A
ENST00000354650.7:c.-395G>A MANE Select	ENSP00000346671.3:n.-395G>A
ENST00000368678.8:c.-325G>A	ENSP00000357667.4:n.-325G>A
ENST00000484067.6:c.-361+30G>A	ENSP00000428983.1:n.-361+30G>A
ENST00000518295.5:c.-512G>A	ENSP00000428695.1:n.-512G>A
ENST00000523238.5:c.-354G>A	ENSP00000430364.1:n.-354G>A
NM_002037.5:c.-395G>A MANE Select	NP_002028.1:n.-395G>A
XM_005266890.2:c.-395G>A	XP_005266947.1:n.-395G>A
XM_005266892.2:c.-395G>A	XP_005266949.1:n.-395G>A
XM_011535662.1:c.-395G>A	XP_011533964.1:n.-395G>A
XM_011535663.1:c.-354G>A	XP_011533965.1:n.-354G>A
XM_011536304.1:c.509C>T	XP_011534606.1:p.Ala170Val
XM_024446614.1:c.509C>T	XP_024302382.1:p.Ala170Val