Canonical Allele Identifier: CA576044698

Gene: SEMA3D

Linked Data

• dbSNP Id: rs1438594093
• gnomAD v2: 7-84713751-A-C
• gnomAD v3: 7-85084435-A-C
• gnomAD v4: 7-85084435-A-C
• MyVariant Identifiers: chr7:g.84713751A>C (hg19) ; chr7:g.85084435A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.85084435A>C , CM000669.2:g.85084435A>C	GRCh38
NC_000007.13:g.84713751A>C , CM000669.1:g.84713751A>C	GRCh37
NC_000007.12:g.84551687A>C	NCBI36
NG_051329.1:g.107421T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284136.11:c.313-2856T>G MANE Select	ENSP00000284136.6:n.313-2856T>G
ENST00000284136.10:c.313-2856T>G	ENSP00000284136.6:n.313-2856T>G
ENST00000444867.1:c.313-2856T>G	ENSP00000401366.1:n.313-2856T>G
NM_152754.2:c.313-2856T>G	NP_689967.2:n.313-2856T>G
XM_011515960.1:c.313-2856T>G	XP_011514262.1:n.313-2856T>G
XM_011515961.1:c.-270-2856T>G	XP_011514263.1:n.-270-2856T>G
XM_011515961.2:c.-270-2856T>G	XP_011514263.1:n.-270-2856T>G
XM_017011873.1:c.313-2856T>G	XP_016867362.1:n.313-2856T>G
NM_001384900.1:c.313-2856T>G MANE Select	NP_001371829.1:n.313-2856T>G
NM_001384901.1:c.313-2856T>G	NP_001371830.1:n.313-2856T>G
NM_001384902.1:c.313-2856T>G	NP_001371831.1:n.313-2856T>G
NM_001384903.1:c.313-2856T>G	NP_001371832.1:n.313-2856T>G
NM_152754.3:c.313-2856T>G	NP_689967.2:n.313-2856T>G