Canonical Allele Identifier: CA839890385
Gene: FSCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1446664551
gnomAD v3: 7-5603198-G-A
gnomAD v4: 7-5603198-G-A
MyVariant Identifiers: chr7:g.5642829G>A (hg19) chr7:g.5603198G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603198G>A , CM000669.2:g.5603198G>A GRCh38
NC_000007.13:g.5642829G>A , CM000669.1:g.5642829G>A GRCh37
NC_000007.12:g.5609355G>A NCBI36
NG_030004.1:g.15394G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-59G>A MANE Select ENSP00000371798.3:n.833-59G>A
ENST00000382361.7:c.833-59G>A ENSP00000371798.3:n.833-59G>A
ENST00000405801.2:c.-2-59G>A ENSP00000383982.2:n.-2-59G>A
ENST00000444748.5:c.-2-59G>A ENSP00000404506.1:n.-2-59G>A
ENST00000447103.5:c.-2-59G>A ENSP00000409967.1:n.-2-59G>A
ENST00000473330.1:n.327G>A
NM_003088.3:c.833-59G>A NP_003079.1:n.833-59G>A
NM_003088.4:c.833-59G>A MANE Select NP_003079.1:n.833-59G>A
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