Canonical Allele Identifier: CA153233225
Gene: FSCN1 HGNC NCBI

Linked Data

dbSNP Id: rs559607054
gnomAD v2: 7-5642800-G-A
gnomAD v3: 7-5603169-G-A
gnomAD v4: 7-5603169-G-A
MyVariant Identifiers: chr7:g.5642800G>A (hg19) chr7:g.5603169G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603169G>A , CM000669.2:g.5603169G>A GRCh38
NC_000007.13:g.5642800G>A , CM000669.1:g.5642800G>A GRCh37
NC_000007.12:g.5609326G>A NCBI36
NG_030004.1:g.15365G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-88G>A MANE Select ENSP00000371798.3:n.833-88G>A
ENST00000382361.7:c.833-88G>A ENSP00000371798.3:n.833-88G>A
ENST00000405801.2:c.-2-88G>A ENSP00000383982.2:n.-2-88G>A
ENST00000444748.5:c.-2-88G>A ENSP00000404506.1:n.-2-88G>A
ENST00000447103.5:c.-2-88G>A ENSP00000409967.1:n.-2-88G>A
ENST00000473330.1:n.298G>A
NM_003088.3:c.833-88G>A NP_003079.1:n.833-88G>A
NM_003088.4:c.833-88G>A MANE Select NP_003079.1:n.833-88G>A
Search 100 bp 5'
Search 100 bp 3'