Canonical Allele Identifier: CA1680910759
Gene: SMOC2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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