Canonical Allele Identifier: CA575901866

Gene: SEMA3C

Linked Data

• dbSNP Id: rs1223122078
• gnomAD v2: 7-80532063-A-G
• gnomAD v3: 7-80902747-A-G
• gnomAD v4: 7-80902747-A-G
• MyVariant Identifiers: chr7:g.80532063A>G (hg19) ; chr7:g.80902747A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902747A>G , CM000669.2:g.80902747A>G	GRCh38
NC_000007.13:g.80532063A>G , CM000669.1:g.80532063A>G	GRCh37
NC_000007.12:g.80369999A>G	NCBI36
NG_054744.1:g.24633T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265361.8:c.103+13932T>C MANE Select	ENSP00000265361.3:n.103+13932T>C
ENST00000265361.7:c.103+13932T>C	ENSP00000265361.3:n.103+13932T>C
ENST00000411788.5:c.191+3082T>C	ENSP00000395398.1:n.191+3082T>C
ENST00000419255.6:c.103+13932T>C	ENSP00000411193.2:n.103+13932T>C
ENST00000427167.5:c.191+3082T>C	ENSP00000399891.1:n.191+3082T>C
ENST00000458729.5:c.103+13932T>C	ENSP00000393825.1:n.103+13932T>C
ENST00000487621.5:n.496+13932T>C
NM_006379.3:c.103+13932T>C	NP_006370.1:n.103+13932T>C
XM_005250113.1:c.-72+3082T>C	XP_005250170.1:n.-72+3082T>C
NM_001350120.1:c.157+13932T>C	NP_001337049.1:n.157+13932T>C
NM_001350121.1:c.-72+3082T>C	NP_001337050.1:n.-72+3082T>C
NM_006379.4:c.103+13932T>C	NP_006370.1:n.103+13932T>C
NM_006379.5:c.103+13932T>C MANE Select	NP_006370.1:n.103+13932T>C
NM_001350120.2:c.157+13932T>C	NP_001337049.1:n.157+13932T>C
NM_001350121.2:c.-72+3082T>C	NP_001337050.1:n.-72+3082T>C