Canonical Allele Identifier: CA1097143631
Gene: SMOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1783865319

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.168540966C>G , CM000668.2:g.168540966C>G GRCh38
NC_000006.11:g.168941646C>G , CM000668.1:g.168941646C>G GRCh37
NC_000006.10:g.168684495C>G NCBI36
NG_032781.1:g.104816C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000356284.7:c.464-2659C>G MANE Select ENSP00000348630.3:n.464-2659C>G
ENST00000354536.9:c.464-2659C>G ENSP00000346537.5:n.464-2659C>G
ENST00000356284.6:c.464-2659C>G ENSP00000348630.2:n.464-2659C>G
NM_001166412.1:c.464-2659C>G NP_001159884.1:n.464-2659C>G
NM_022138.2:c.464-2659C>G NP_071421.1:n.464-2659C>G
XM_011536065.1:c.464-2659C>G XP_011534367.1:n.464-2659C>G
XM_011536066.1:c.464-2659C>G XP_011534368.1:n.464-2659C>G
NM_001166412.2:c.464-2659C>G MANE Select NP_001159884.1:n.464-2659C>G
NM_022138.3:c.464-2659C>G NP_071421.1:n.464-2659C>G