Canonical Allele Identifier: CA572249534

Gene: SMOC2

Linked Data

• dbSNP Id: rs761341351
• gnomAD v2: 6-168941573-C-A
• gnomAD v3: 6-168540893-C-A
• gnomAD v4: 6-168540893-C-A
• MyVariant Identifiers: chr6:g.168941573C>A (hg19) ; chr6:g.168540893C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.168540893C>A , CM000668.2:g.168540893C>A	GRCh38
NC_000006.11:g.168941573C>A , CM000668.1:g.168941573C>A	GRCh37
NC_000006.10:g.168684422C>A	NCBI36
NG_032781.1:g.104743C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356284.7:c.464-2732C>A MANE Select	ENSP00000348630.3:n.464-2732C>A
ENST00000354536.9:c.464-2732C>A	ENSP00000346537.5:n.464-2732C>A
ENST00000356284.6:c.464-2732C>A	ENSP00000348630.2:n.464-2732C>A
NM_001166412.1:c.464-2732C>A	NP_001159884.1:n.464-2732C>A
NM_022138.2:c.464-2732C>A	NP_071421.1:n.464-2732C>A
XM_011536065.1:c.464-2732C>A	XP_011534367.1:n.464-2732C>A
XM_011536066.1:c.464-2732C>A	XP_011534368.1:n.464-2732C>A
NM_001166412.2:c.464-2732C>A MANE Select	NP_001159884.1:n.464-2732C>A
NM_022138.3:c.464-2732C>A	NP_071421.1:n.464-2732C>A