Canonical Allele Identifier: CA2676181413
Gene: SGCD HGNC NCBI

Linked Data

gnomAD v4: 5-156766800-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156766800A>G , CM000667.2:g.156766800A>G GRCh38
NC_000005.9:g.156193811A>G , CM000667.1:g.156193811A>G GRCh37
NC_000005.8:g.156126389A>G NCBI36
NG_008693.2:g.901458A>G , LRG_205:g.901458A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.*7410A>G MANE Select ENSP00000338343.4:n.*7410A>G
ENST00000435422.7:c.*7410A>G ENSP00000403003.2:n.*7410A>G
NM_000337.5:c.*7410A>G , LRG_205t1:c.*7410A>G NP_000328.2:n.*7410A>G
NM_001128209.1:c.*7410A>G NP_001121681.1:n.*7410A>G
XM_005265966.3:c.*7410A>G XP_005266023.1:n.*7410A>G
XM_006714911.2:c.*7410A>G XP_006714974.1:n.*7410A>G
XM_011534621.1:c.*7410A>G XP_011532923.1:n.*7410A>G
NM_001128209.2:c.*7410A>G NP_001121681.1:n.*7410A>G
NM_000337.6:c.*7410A>G MANE Select NP_000328.2:n.*7410A>G
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