Canonical Allele Identifier: CA144972556
Gene: FYN HGNC NCBI

Linked Data

dbSNP Id: rs552626026
gnomAD v2: 6-112194344-T-C
gnomAD v3: 6-111873141-T-C
gnomAD v4: 6-111873141-T-C
MyVariant Identifiers: chr6:g.112194344T>C (hg19) chr6:g.112194344_112194372delinsCGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg19) chr6:g.111873141T>C (hg38) chr6:g.111873141_111873169delinsCGGCGCGGGCGGCGGCCGCCGGGCGGTGC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.111873141T>C , CM000668.2:g.111873141T>C GRCh38
NC_000006.11:g.112194344T>C , CM000668.1:g.112194344T>C GRCh37
NC_000006.10:g.112301037T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368682.8:c.-296A>G ENSP00000357671.3:n.-296A>G
ENST00000354650.7:c.-296A>G MANE Select ENSP00000346671.3:n.-296A>G
ENST00000368678.8:c.-226A>G ENSP00000357667.4:n.-226A>G
ENST00000484067.6:c.-296A>G ENSP00000428983.1:n.-296A>G
ENST00000518295.5:c.-413A>G ENSP00000428695.1:n.-413A>G
ENST00000523238.5:c.-255A>G ENSP00000430364.1:n.-255A>G
NM_002037.5:c.-296A>G MANE Select NP_002028.1:n.-296A>G
XM_005266890.2:c.-296A>G XP_005266947.1:n.-296A>G
XM_005266892.2:c.-296A>G XP_005266949.1:n.-296A>G
XM_011535662.1:c.-296A>G XP_011533964.1:n.-296A>G
XM_011535663.1:c.-255A>G XP_011533965.1:n.-255A>G
XM_011536304.1:c.410T>C XP_011534606.1:p.Leu137Pro
XM_024446614.1:c.410T>C XP_024302382.1:p.Leu137Pro
Search 100 bp 5'
Search 100 bp 3'