Canonical Allele Identifier: CA1667372010
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs1778274783
gnomAD v4: 6-139372798-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372798T>C , CM000668.2:g.139372798T>C GRCh38
NC_000006.11:g.139693935T>C , CM000668.1:g.139693935T>C GRCh37
NC_000006.10:g.139735628T>C NCBI36
NG_016169.1:g.6851A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*334A>G MANE Select ENSP00000356623.2:n.*334A>G
ENST00000367651.3:c.*334A>G ENSP00000356623.2:n.*334A>G
ENST00000536159.2:c.*334A>G ENSP00000442831.1:n.*334A>G
ENST00000537332.2:c.*334A>G ENSP00000444198.2:n.*334A>G
NM_001168388.2:c.*334A>G NP_001161860.1:n.*334A>G
NM_001168389.2:c.*334A>G NP_001161861.2:n.*334A>G
NM_006079.4:c.*334A>G NP_006070.2:n.*334A>G
NM_006079.5:c.*334A>G MANE Select NP_006070.2:n.*334A>G
NM_001168388.3:c.*334A>G NP_001161860.1:n.*334A>G
NM_001168389.3:c.*334A>G NP_001161861.2:n.*334A>G
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