Canonical Allele Identifier: CA650603282
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967286A>G , CM000667.2:g.155967286A>G GRCh38
NC_000005.9:g.155394296A>G , CM000667.1:g.155394296A>G GRCh37
NC_000005.8:g.155326874A>G NCBI36
NG_008693.2:g.101943A>G , LRG_205:g.101943A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96862A>G ENSP00000429378.1:n.-282+96862A>G
XM_017009723.2:c.-208+96862A>G XP_016865212.1:n.-208+96862A>G
XM_017009724.1:c.-207-156570A>G XP_016865213.1:n.-207-156570A>G