Canonical Allele Identifier: CA1556466094
Gene: SV2C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76191482G= , CM000667.2:g.76191482G= GRCh38
NC_000005.9:g.75487307G= , CM000667.1:g.75487307G= GRCh37
NC_000005.8:g.75523063G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502798.7:c.581-3437G= MANE Select ENSP00000423541.2:n.581-3437G=
ENST00000322285.7:c.581-3437G= ENSP00000316983.7:n.581-3437G=
ENST00000502798.6:c.581-3437G= ENSP00000423541.2:n.581-3437G=
NM_001297716.1:c.581-3437G= NP_001284645.1:n.581-3437G=
NM_014979.3:c.581-3437G= NP_055794.3:n.581-3437G=
XM_011543281.1:c.581-3437G= XP_011541583.1:n.581-3437G=
XM_011543282.1:c.9-18254G= XP_011541584.1:n.9-18254G=
XM_011543281.3:c.581-3437G= XP_011541583.1:n.581-3437G=
XM_011543282.3:c.581-3437G= XP_011541584.2:n.581-3437G=
NM_014979.4:c.581-3437G= MANE Select NP_055794.3:n.581-3437G=
NM_001297716.2:c.581-3437G= NP_001284645.1:n.581-3437G=