Canonical Allele Identifier: CA10623848
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 352346
ClinVar RCV Id: RCV000289713 RCV000333984
dbSNP Id: rs886060291
gnomAD v3: 5-156760157-A-T
gnomAD v4: 5-156760157-A-T
MyVariant Identifiers: chr5:g.156187168A>T (hg19) chr5:g.156760157A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156760157A>T , CM000667.2:g.156760157A>T GRCh38
NC_000005.9:g.156187168A>T , CM000667.1:g.156187168A>T GRCh37
NC_000005.8:g.156119746A>T NCBI36
NG_008693.2:g.894815A>T , LRG_205:g.894815A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.*767A>T MANE Select ENSP00000338343.4:n.*767A>T
ENST00000435422.7:c.*767A>T ENSP00000403003.2:n.*767A>T
NM_000337.5:c.*767A>T , LRG_205t1:c.*767A>T NP_000328.2:n.*767A>T
NM_001128209.1:c.*767A>T NP_001121681.1:n.*767A>T
XM_005265966.3:c.*767A>T XP_005266023.1:n.*767A>T
XM_006714911.2:c.*767A>T XP_006714974.1:n.*767A>T
XM_011534621.1:c.*767A>T XP_011532923.1:n.*767A>T
NM_001128209.2:c.*767A>T NP_001121681.1:n.*767A>T
NM_000337.6:c.*767A>T MANE Select NP_000328.2:n.*767A>T
Search 100 bp 5'
Search 100 bp 3'