Canonical Allele Identifier: CA2481403190
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202597010C= , CM000663.2:g.202597010C= GRCh38
NC_000001.10:g.202566138C= , CM000663.1:g.202566138C= GRCh37
NC_000001.9:g.200832761C= NCBI36
NG_041776.1:g.118414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1054-47G= MANE Select ENSP00000356237.4:n.1054-47G=
ENST00000367267.5:c.1054-47G= ENSP00000356236.1:n.1054-47G=
ENST00000367268.4:c.1054-47G= ENSP00000356237.4:n.1054-47G=
NM_001136504.1:c.1054-47G= NP_001129976.1:n.1054-47G=
NM_177402.4:c.1054-47G= NP_796376.2:n.1054-47G=
XM_011509192.1:c.1063-47G= XP_011507494.1:n.1063-47G=
XR_922430.1:n.34C=
XM_011509192.2:c.1063-47G= XP_011507494.1:n.1063-47G=
XM_017000309.2:c.1234-47G= XP_016855798.1:n.1234-47G=
XM_017000310.2:c.1225-47G= XP_016855799.1:n.1225-47G=
XM_017000311.2:c.1063-47G= XP_016855800.1:n.1063-47G=
XM_017000312.1:c.1063-47G= XP_016855801.1:n.1063-47G=
XM_017000313.1:c.1054-47G= XP_016855802.1:n.1054-47G=
NM_177402.5:c.1054-47G= MANE Select NP_796376.2:n.1054-47G=