Canonical Allele Identifier: CA102346812

Gene: UNC5C

Linked Data

• dbSNP Id: rs922990378
• MyVariant Identifiers: chr4:g.96458469T>C (hg19) ; chr4:g.95537318T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.95537318T>C , CM000666.2:g.95537318T>C	GRCh38
NC_000004.11:g.96458469T>C , CM000666.1:g.96458469T>C	GRCh37
NC_000004.10:g.96677492T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000453304.6:c.124+11416A>G MANE Select	ENSP00000406022.1:n.124+11416A>G
ENST00000453304.5:c.124+11416A>G	ENSP00000406022.1:n.124+11416A>G
ENST00000504962.1:c.124+11416A>G	ENSP00000425117.1:n.124+11416A>G
ENST00000506749.5:c.124+11416A>G	ENSP00000426153.1:n.124+11416A>G
ENST00000513796.5:c.124+11416A>G	ENSP00000426924.1:n.124+11416A>G
NM_003728.3:c.124+11416A>G	NP_003719.3:n.124+11416A>G
XM_005263321.2:c.124+11416A>G	XP_005263378.1:n.124+11416A>G
XM_005263321.3:c.124+11416A>G	XP_005263378.1:n.124+11416A>G
NM_003728.4:c.124+11416A>G MANE Select	NP_003719.3:n.124+11416A>G