Canonical Allele Identifier: CA161771189

Gene: SEMA3A

Linked Data

• dbSNP Id: rs940298902
• gnomAD v2: 7-83656810-C-G
• gnomAD v3: 7-84027494-C-G
• gnomAD v4: 7-84027494-C-G
• MyVariant Identifiers: chr7:g.83656810C>G (hg19) ; chr7:g.84027494C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.84027494C>G , CM000669.2:g.84027494C>G	GRCh38
NC_000007.13:g.83656810C>G , CM000669.1:g.83656810C>G	GRCh37
NC_000007.12:g.83494746C>G	NCBI36
NG_011489.1:g.172408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265362.9:c.668-13143G>C MANE Select	ENSP00000265362.3:n.668-13143G>C
ENST00000265362.8:c.668-13143G>C	ENSP00000265362.3:n.668-13143G>C
ENST00000436949.5:c.668-13143G>C	ENSP00000415260.1:n.668-13143G>C
NM_006080.2:c.668-13143G>C	NP_006071.1:n.668-13143G>C
XM_005250110.2:c.668-13143G>C	XP_005250167.1:n.668-13143G>C
XM_005250111.3:c.668-13143G>C	XP_005250168.1:n.668-13143G>C
XM_006715839.2:c.668-13143G>C	XP_006715902.1:n.668-13143G>C
XM_011515734.1:c.668-13143G>C	XP_011514036.1:n.668-13143G>C
XM_011515735.1:c.668-13143G>C	XP_011514037.1:n.668-13143G>C
XM_005250110.3:c.668-13143G>C	XP_005250167.1:n.668-13143G>C
XM_005250111.4:c.668-13143G>C	XP_005250168.1:n.668-13143G>C
XM_006715839.3:c.668-13143G>C	XP_006715902.1:n.668-13143G>C
XM_011515734.3:c.668-13143G>C	XP_011514036.1:n.668-13143G>C
XM_017011673.1:c.668-13143G>C	XP_016867162.1:n.668-13143G>C
XM_024446633.1:c.668-13143G>C	XP_024302401.1:n.668-13143G>C
NM_006080.3:c.668-13143G>C MANE Select	NP_006071.1:n.668-13143G>C