Canonical Allele Identifier: CA817295328

Gene: FYN

Linked Data

• dbSNP Id: rs1172757854
• gnomAD v4: 6-111873146-C-A
• MyVariant Identifiers: chr6:g.112194349C>A (hg19) ; chr6:g.111873146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873146C>A , CM000668.2:g.111873146C>A	GRCh38
NC_000006.11:g.112194349C>A , CM000668.1:g.112194349C>A	GRCh37
NC_000006.10:g.112301042C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-301G>T	ENSP00000357671.3:n.-301G>T
ENST00000354650.7:c.-301G>T MANE Select	ENSP00000346671.3:n.-301G>T
ENST00000368678.8:c.-231G>T	ENSP00000357667.4:n.-231G>T
ENST00000484067.6:c.-301G>T	ENSP00000428983.1:n.-301G>T
ENST00000518295.5:c.-418G>T	ENSP00000428695.1:n.-418G>T
ENST00000523238.5:c.-260G>T	ENSP00000430364.1:n.-260G>T
NM_002037.5:c.-301G>T MANE Select	NP_002028.1:n.-301G>T
XM_005266890.2:c.-301G>T	XP_005266947.1:n.-301G>T
XM_005266892.2:c.-301G>T	XP_005266949.1:n.-301G>T
XM_011535662.1:c.-301G>T	XP_011533964.1:n.-301G>T
XM_011535663.1:c.-260G>T	XP_011533965.1:n.-260G>T
XM_011536304.1:c.415C>A	XP_011534606.1:p.Arg139=
XM_024446614.1:c.415C>A	XP_024302382.1:p.Arg139=