Canonical Allele Identifier: CA341502034
Gene: CELSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1346539715

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264503G>A , CM000663.2:g.109264503G>A GRCh38
NC_000001.10:g.109807125G>A , CM000663.1:g.109807125G>A GRCh37
NC_000001.9:g.109608648G>A NCBI36
NG_052669.1:g.19799G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5339G>A MANE Select ENSP00000271332.3:p.Ser1780Asn
ENST00000271332.3:c.5339G>A ENSP00000271332.3:p.Ser1780Asn
NM_001408.2:c.5339G>A NP_001399.1:p.Ser1780Asn
XM_005270580.3:c.5339G>A XP_005270637.1:p.Ser1780Asn
NM_001408.3:c.5339G>A MANE Select NP_001399.1:p.Ser1780Asn