Canonical Allele Identifier: CA843050083

Gene: SEMA3A

Linked Data

• dbSNP Id: rs1466687436
• gnomAD v3: 7-84027441-G-T
• gnomAD v4: 7-84027441-G-T
• MyVariant Identifiers: chr7:g.83656757G>T (hg19) ; chr7:g.84027441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84027441G>T , CM000669.2:g.84027441G>T	GRCh38
NC_000007.13:g.83656757G>T , CM000669.1:g.83656757G>T	GRCh37
NC_000007.12:g.83494693G>T	NCBI36
NG_011489.1:g.172461C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265362.9:c.668-13090C>A MANE Select	ENSP00000265362.3:n.668-13090C>A
ENST00000265362.8:c.668-13090C>A	ENSP00000265362.3:n.668-13090C>A
ENST00000436949.5:c.668-13090C>A	ENSP00000415260.1:n.668-13090C>A
NM_006080.2:c.668-13090C>A	NP_006071.1:n.668-13090C>A
XM_005250110.2:c.668-13090C>A	XP_005250167.1:n.668-13090C>A
XM_005250111.3:c.668-13090C>A	XP_005250168.1:n.668-13090C>A
XM_006715839.2:c.668-13090C>A	XP_006715902.1:n.668-13090C>A
XM_011515734.1:c.668-13090C>A	XP_011514036.1:n.668-13090C>A
XM_011515735.1:c.668-13090C>A	XP_011514037.1:n.668-13090C>A
XM_005250110.3:c.668-13090C>A	XP_005250167.1:n.668-13090C>A
XM_005250111.4:c.668-13090C>A	XP_005250168.1:n.668-13090C>A
XM_006715839.3:c.668-13090C>A	XP_006715902.1:n.668-13090C>A
XM_011515734.3:c.668-13090C>A	XP_011514036.1:n.668-13090C>A
XM_017011673.1:c.668-13090C>A	XP_016867162.1:n.668-13090C>A
XM_024446633.1:c.668-13090C>A	XP_024302401.1:n.668-13090C>A
NM_006080.3:c.668-13090C>A MANE Select	NP_006071.1:n.668-13090C>A