Canonical Allele Identifier: CA1655112502
Gene: FYN HGNC NCBI

Linked Data

dbSNP Id: rs1296890249

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111873142G>C , CM000668.2:g.111873142G>C GRCh38
NC_000006.11:g.112194345G>C , CM000668.1:g.112194345G>C GRCh37
NC_000006.10:g.112301038G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368682.8:c.-297C>G ENSP00000357671.3:n.-297C>G
ENST00000354650.7:c.-297C>G MANE Select ENSP00000346671.3:n.-297C>G
ENST00000368678.8:c.-227C>G ENSP00000357667.4:n.-227C>G
ENST00000484067.6:c.-297C>G ENSP00000428983.1:n.-297C>G
ENST00000518295.5:c.-414C>G ENSP00000428695.1:n.-414C>G
ENST00000523238.5:c.-256C>G ENSP00000430364.1:n.-256C>G
NM_002037.5:c.-297C>G MANE Select NP_002028.1:n.-297C>G
XM_005266890.2:c.-297C>G XP_005266947.1:n.-297C>G
XM_005266892.2:c.-297C>G XP_005266949.1:n.-297C>G
XM_011535662.1:c.-297C>G XP_011533964.1:n.-297C>G
XM_011535663.1:c.-256C>G XP_011533965.1:n.-256C>G
XM_011536304.1:c.411G>C XP_011534606.1:p.Leu137=
XM_024446614.1:c.411G>C XP_024302382.1:p.Leu137=