Canonical Allele Identifier: CA356878128
Gene: SGCB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.52899760A>C (hg19) chr4:g.52033594A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033594A>C , CM000666.2:g.52033594A>C GRCh38
NC_000004.11:g.52899760A>C , CM000666.1:g.52899760A>C GRCh37
NC_000004.10:g.52594517A>C NCBI36
NG_008891.1:g.9726T>G , LRG_204:g.9726T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.80T>G MANE Select ENSP00000370839.6:p.Val27Gly
ENST00000381431.9:c.80T>G ENSP00000370839.5:p.Val27Gly
ENST00000506357.5:c.66T>G
ENST00000514133.1:c.47T>G ENSP00000425818.1:p.Val16Gly
NM_000232.4:c.80T>G , LRG_204t1:c.80T>G NP_000223.1:p.Val27Gly
XM_011534403.1:c.34-3731T>G XP_011532705.1:n.34-3731T>G
NM_000232.5:c.80T>G MANE Select NP_000223.1:p.Val27Gly
Search 100 bp 5'
Search 100 bp 3'