Canonical Allele Identifier: CA1804458190
Gene: SDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96610720A= , CM000670.2:g.96610720A= GRCh38
NC_000008.10:g.97622948A= , CM000670.1:g.97622948A= GRCh37
NC_000008.9:g.97692124A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002998.4:c.*1172A= MANE Select NP_002989.2:n.*1172A=
ENST00000302190.9:c.*1172A= MANE Select ENSP00000307046.4:n.*1172A=
NM_002998.3:c.*1172A= NP_002989.2:n.*1172A=
ENST00000302190.8:c.*1172A= ENSP00000307046.4:n.*1172A=
XM_005251019.3:c.*1172A= XP_005251076.1:n.*1172A=
XM_005251020.2:c.*1172A= XP_005251077.1:n.*1172A=
XM_006716614.2:c.*1172A= XP_006716677.2:n.*1172A=
XM_011517211.1:c.*1172A= XP_011515513.1:n.*1172A=
XM_011517212.1:c.*1172A= XP_011515514.1:n.*1172A=
XM_011517212.3:c.*1172A= XP_011515514.1:n.*1172A=
XM_024447228.1:c.*1172A= XP_024302996.1:n.*1172A=