Canonical Allele Identifier: CA806083443
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1435332874
gnomAD v3: 5-155967241-T-C
gnomAD v4: 5-155967241-T-C
MyVariant Identifiers: chr5:g.155394251T>C (hg19) chr5:g.155967241T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967241T>C , CM000667.2:g.155967241T>C GRCh38
NC_000005.9:g.155394251T>C , CM000667.1:g.155394251T>C GRCh37
NC_000005.8:g.155326829T>C NCBI36
NG_008693.2:g.101898T>C , LRG_205:g.101898T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96817T>C ENSP00000429378.1:n.-282+96817T>C
XM_017009723.2:c.-208+96817T>C XP_016865212.1:n.-208+96817T>C
XM_017009724.1:c.-207-156615T>C XP_016865213.1:n.-207-156615T>C
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