Canonical Allele Identifier: CA1556466081
Gene: SV2C HGNC NCBI

Linked Data

dbSNP Id: rs1744101644
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76191465T>A , CM000667.2:g.76191465T>A GRCh38
NC_000005.9:g.75487290T>A , CM000667.1:g.75487290T>A GRCh37
NC_000005.8:g.75523046T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502798.7:c.581-3454T>A MANE Select ENSP00000423541.2:n.581-3454T>A
ENST00000322285.7:c.581-3454T>A ENSP00000316983.7:n.581-3454T>A
ENST00000502798.6:c.581-3454T>A ENSP00000423541.2:n.581-3454T>A
NM_001297716.1:c.581-3454T>A NP_001284645.1:n.581-3454T>A
NM_014979.3:c.581-3454T>A NP_055794.3:n.581-3454T>A
XM_011543281.1:c.581-3454T>A XP_011541583.1:n.581-3454T>A
XM_011543282.1:c.9-18271T>A XP_011541584.1:n.9-18271T>A
XM_011543281.3:c.581-3454T>A XP_011541583.1:n.581-3454T>A
XM_011543282.3:c.581-3454T>A XP_011541584.2:n.581-3454T>A
NM_014979.4:c.581-3454T>A MANE Select NP_055794.3:n.581-3454T>A
NM_001297716.2:c.581-3454T>A NP_001284645.1:n.581-3454T>A
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