Canonical Allele Identifier: CA130550295
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs982522491
gnomAD v3: 5-155967272-C-T
gnomAD v4: 5-155967272-C-T
MyVariant Identifiers: chr5:g.155394282C>T (hg19) chr5:g.155967272C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.155967272C>T , CM000667.2:g.155967272C>T GRCh38
NC_000005.9:g.155394282C>T , CM000667.1:g.155394282C>T GRCh37
NC_000005.8:g.155326860C>T NCBI36
NG_008693.2:g.101929C>T , LRG_205:g.101929C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517913.5:c.-282+96848C>T ENSP00000429378.1:n.-282+96848C>T
XM_017009723.2:c.-208+96848C>T XP_016865212.1:n.-208+96848C>T
XM_017009724.1:c.-207-156584C>T XP_016865213.1:n.-207-156584C>T
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