Canonical Allele Identifier: CA1083260941
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967329A>C , CM000667.2:g.155967329A>C GRCh38
NC_000005.9:g.155394339A>C , CM000667.1:g.155394339A>C GRCh37
NC_000005.8:g.155326917A>C NCBI36
NG_008693.2:g.101986A>C , LRG_205:g.101986A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96905A>C ENSP00000429378.1:n.-282+96905A>C
XM_017009723.2:c.-208+96905A>C XP_016865212.1:n.-208+96905A>C
XM_017009724.1:c.-207-156527A>C XP_016865213.1:n.-207-156527A>C