Canonical Allele Identifier: CA341502031
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264502A>C , CM000663.2:g.109264502A>C GRCh38
NC_000001.10:g.109807124A>C , CM000663.1:g.109807124A>C GRCh37
NC_000001.9:g.109608647A>C NCBI36
NG_052669.1:g.19798A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5338A>C MANE Select ENSP00000271332.3:p.Ser1780Arg
ENST00000271332.3:c.5338A>C ENSP00000271332.3:p.Ser1780Arg
NM_001408.2:c.5338A>C NP_001399.1:p.Ser1780Arg
XM_005270580.3:c.5338A>C XP_005270637.1:p.Ser1780Arg
NM_001408.3:c.5338A>C MANE Select NP_001399.1:p.Ser1780Arg