Canonical Allele Identifier: CA569738153

Gene: FYN

Linked Data

• dbSNP Id: rs1160599255
• gnomAD v2: 6-112194342-C-T
• gnomAD v3: 6-111873139-C-T
• gnomAD v4: 6-111873139-C-T
• MyVariant Identifiers: chr6:g.112194342C>T (hg19) ; chr6:g.111873139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873139C>T , CM000668.2:g.111873139C>T	GRCh38
NC_000006.11:g.112194342C>T , CM000668.1:g.112194342C>T	GRCh37
NC_000006.10:g.112301035C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-294G>A	ENSP00000357671.3:n.-294G>A
ENST00000354650.7:c.-294G>A MANE Select	ENSP00000346671.3:n.-294G>A
ENST00000368678.8:c.-224G>A	ENSP00000357667.4:n.-224G>A
ENST00000484067.6:c.-294G>A	ENSP00000428983.1:n.-294G>A
ENST00000518295.5:c.-411G>A	ENSP00000428695.1:n.-411G>A
ENST00000523238.5:c.-253G>A	ENSP00000430364.1:n.-253G>A
NM_002037.5:c.-294G>A MANE Select	NP_002028.1:n.-294G>A
XM_005266890.2:c.-294G>A	XP_005266947.1:n.-294G>A
XM_005266892.2:c.-294G>A	XP_005266949.1:n.-294G>A
XM_011535662.1:c.-294G>A	XP_011533964.1:n.-294G>A
XM_011535663.1:c.-253G>A	XP_011533965.1:n.-253G>A
XM_011536304.1:c.408C>T	XP_011534606.1:p.Ser136=
XM_024446614.1:c.408C>T	XP_024302382.1:p.Ser136=