Canonical Allele Identifier: CA2246157923
Gene: HES7 HGNC NCBI

Linked Data

dbSNP Id: rs1981243061
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8120703C>G , CM000679.2:g.8120703C>G GRCh38
NC_000017.10:g.8024021C>G , CM000679.1:g.8024021C>G GRCh37
NC_000017.9:g.7964746C>G NCBI36
NG_015807.1:g.3214G>C
NG_015816.1:g.8390G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000541682.7:c.*868G>C MANE Select ENSP00000446205.2:n.*868G>C
ENST00000541682.6:c.1561G>C ENSP00000446205.2:n.1561G>C
NM_001165967.1:c.*868G>C NP_001159439.1:n.*868G>C
NM_032580.3:c.*868G>C NP_115969.2:n.*868G>C
XM_011524038.1:c.*868G>C XP_011522340.1:n.*868G>C
XR_934203.1:n.69+889C>G
XM_017025232.1:c.*868G>C XP_016880721.1:n.*868G>C
XM_024451007.1:c.*868G>C XP_024306775.1:n.*868G>C
NM_001165967.2:c.*868G>C MANE Select NP_001159439.1:n.*868G>C
NM_032580.4:c.*868G>C NP_115969.2:n.*868G>C
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