Canonical Allele Identifier: CA10619828
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 352442
ClinVar RCV Id: RCV000321589 RCV000378458
dbSNP Id: rs150418759
gnomAD v2: 5-156193922-G-A
gnomAD v3: 5-156766911-G-A
gnomAD v4: 5-156766911-G-A
MyVariant Identifiers: chr5:g.156193922G>A (hg19) chr5:g.156766911G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156766911G>A , CM000667.2:g.156766911G>A GRCh38
NC_000005.9:g.156193922G>A , CM000667.1:g.156193922G>A GRCh37
NC_000005.8:g.156126500G>A NCBI36
NG_008693.2:g.901569G>A , LRG_205:g.901569G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.*7521G>A MANE Select ENSP00000338343.4:n.*7521G>A
ENST00000435422.7:c.*7521G>A ENSP00000403003.2:n.*7521G>A
NM_000337.5:c.*7521G>A , LRG_205t1:c.*7521G>A NP_000328.2:n.*7521G>A
NM_001128209.1:c.*7521G>A NP_001121681.1:n.*7521G>A
XM_005265966.3:c.*7521G>A XP_005266023.1:n.*7521G>A
XM_006714911.2:c.*7521G>A XP_006714974.1:n.*7521G>A
XM_011534621.1:c.*7521G>A XP_011532923.1:n.*7521G>A
NM_001128209.2:c.*7521G>A NP_001121681.1:n.*7521G>A
NM_000337.6:c.*7521G>A MANE Select NP_000328.2:n.*7521G>A
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