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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA356878684
Gene: SGCB
HGNC
NCBI
Linked Data
gnomAD v4:
4-52038235-C-A
MyVariant Identifiers:
chr4:g.52904401C>A (hg19)
chr4:g.52038235C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.52038235C>A , CM000666.2:g.52038235C>A
GRCh38
NC_000004.11:g.52904401C>A , CM000666.1:g.52904401C>A
GRCh37
NC_000004.10:g.52599158C>A
NCBI36
NG_008891.1:g.5085G>T , LRG_204:g.5085G>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000381431.10:c.25G>T
MANE Select
ENSP00000370839.6:p.Ala9Ser
ENST00000381431.9:c.25G>T
ENSP00000370839.5:p.Ala9Ser
ENST00000506357.5:c.11G>T
NM_000232.4:c.25G>T , LRG_204t1:c.25G>T
NP_000223.1:p.Ala9Ser
XM_011534403.1:c.25G>T
XP_011532705.1:p.Ala9Ser
NM_000232.5:c.25G>T
MANE Select
NP_000223.1:p.Ala9Ser
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