Canonical Allele Identifier: CA822372450

Gene: SMOC2

Linked Data

• dbSNP Id: rs1387165230
• MyVariant Identifiers: chr6:g.168941647C>G (hg19) ; chr6:g.168540967C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.168540967C>G , CM000668.2:g.168540967C>G	GRCh38
NC_000006.11:g.168941647C>G , CM000668.1:g.168941647C>G	GRCh37
NC_000006.10:g.168684496C>G	NCBI36
NG_032781.1:g.104817C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356284.7:c.464-2658C>G MANE Select	ENSP00000348630.3:n.464-2658C>G
ENST00000354536.9:c.464-2658C>G	ENSP00000346537.5:n.464-2658C>G
ENST00000356284.6:c.464-2658C>G	ENSP00000348630.2:n.464-2658C>G
NM_001166412.1:c.464-2658C>G	NP_001159884.1:n.464-2658C>G
NM_022138.2:c.464-2658C>G	NP_071421.1:n.464-2658C>G
XM_011536065.1:c.464-2658C>G	XP_011534367.1:n.464-2658C>G
XM_011536066.1:c.464-2658C>G	XP_011534368.1:n.464-2658C>G
NM_001166412.2:c.464-2658C>G MANE Select	NP_001159884.1:n.464-2658C>G
NM_022138.3:c.464-2658C>G	NP_071421.1:n.464-2658C>G