Canonical Allele Identifier: CA102346794

Gene: UNC5C

Linked Data

• dbSNP Id: rs767206930
• gnomAD v3: 4-95537183-A-T
• gnomAD v4: 4-95537183-A-T
• MyVariant Identifiers: chr4:g.96458334A>T (hg19) ; chr4:g.95537183A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537183A>T , CM000666.2:g.95537183A>T	GRCh38
NC_000004.11:g.96458334A>T , CM000666.1:g.96458334A>T	GRCh37
NC_000004.10:g.96677357A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000453304.6:c.124+11551T>A MANE Select	ENSP00000406022.1:n.124+11551T>A
ENST00000453304.5:c.124+11551T>A	ENSP00000406022.1:n.124+11551T>A
ENST00000504962.1:c.124+11551T>A	ENSP00000425117.1:n.124+11551T>A
ENST00000506749.5:c.124+11551T>A	ENSP00000426153.1:n.124+11551T>A
ENST00000513796.5:c.124+11551T>A	ENSP00000426924.1:n.124+11551T>A
NM_003728.3:c.124+11551T>A	NP_003719.3:n.124+11551T>A
XM_005263321.2:c.124+11551T>A	XP_005263378.1:n.124+11551T>A
XM_005263321.3:c.124+11551T>A	XP_005263378.1:n.124+11551T>A
NM_003728.4:c.124+11551T>A MANE Select	NP_003719.3:n.124+11551T>A