Canonical Allele Identifier: CA987477
Gene: CELSR2 HGNC NCBI

Linked Data

dbSNP Id: rs115968305

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264342C>T , CM000663.2:g.109264342C>T GRCh38
NC_000001.10:g.109806964C>T , CM000663.1:g.109806964C>T GRCh37
NC_000001.9:g.109608487C>T NCBI36
NG_052669.1:g.19638C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5266C>T MANE Select ENSP00000271332.3:p.Arg1756Cys
ENST00000271332.3:c.5266C>T ENSP00000271332.3:p.Arg1756Cys
NM_001408.2:c.5266C>T NP_001399.1:p.Arg1756Cys
XM_005270580.3:c.5266C>T XP_005270637.1:p.Arg1756Cys
NM_001408.3:c.5266C>T MANE Select NP_001399.1:p.Arg1756Cys