Canonical Allele Identifier: CA569738145

Gene: FYN

Linked Data

• dbSNP Id: rs563467191
• gnomAD v2: 6-112194248-G-T
• gnomAD v3: 6-111873045-G-T
• gnomAD v4: 6-111873045-G-T
• MyVariant Identifiers: chr6:g.112194248G>T (hg19) ; chr6:g.111873045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873045G>T , CM000668.2:g.111873045G>T	GRCh38
NC_000006.11:g.112194248G>T , CM000668.1:g.112194248G>T	GRCh37
NC_000006.10:g.112300941G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-200C>A	ENSP00000357671.3:n.-200C>A
ENST00000354650.7:c.-200C>A MANE Select	ENSP00000346671.3:n.-200C>A
ENST00000368678.8:c.-130C>A	ENSP00000357667.4:n.-130C>A
ENST00000368682.7:c.-200C>A	ENSP00000357671.3:n.-200C>A
ENST00000484067.6:c.-200C>A	ENSP00000428983.1:n.-200C>A
ENST00000518295.5:c.-317C>A	ENSP00000428695.1:n.-317C>A
ENST00000523238.5:c.-159C>A	ENSP00000430364.1:n.-159C>A
NM_002037.5:c.-200C>A MANE Select	NP_002028.1:n.-200C>A
XM_005266890.2:c.-200C>A	XP_005266947.1:n.-200C>A
XM_005266892.2:c.-200C>A	XP_005266949.1:n.-200C>A
XM_011535662.1:c.-200C>A	XP_011533964.1:n.-200C>A
XM_011535663.1:c.-159C>A	XP_011533965.1:n.-159C>A
XM_011536304.1:c.314G>T	XP_011534606.1:p.Arg105Leu
XM_005266890.4:c.-200C>A	XP_005266947.1:n.-200C>A
XM_005266892.4:c.-200C>A	XP_005266949.1:n.-200C>A
XM_017010655.2:c.-200C>A	XP_016866144.1:n.-200C>A
XM_024446614.1:c.314G>T	XP_024302382.1:p.Arg105Leu
NM_153047.4:c.-200C>A	NP_694592.1:n.-200C>A