Canonical Allele Identifier: CA341502222
Gene: CELSR2 HGNC NCBI

Linked Data

dbSNP Id: rs776084621

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264577A>G , CM000663.2:g.109264577A>G GRCh38
NC_000001.10:g.109807199A>G , CM000663.1:g.109807199A>G GRCh37
NC_000001.9:g.109608722A>G NCBI36
NG_052669.1:g.19873A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5413A>G MANE Select ENSP00000271332.3:p.Asn1805Asp
ENST00000271332.3:c.5413A>G ENSP00000271332.3:p.Asn1805Asp
NM_001408.2:c.5413A>G NP_001399.1:p.Asn1805Asp
XM_005270580.3:c.5413A>G XP_005270637.1:p.Asn1805Asp
NM_001408.3:c.5413A>G MANE Select NP_001399.1:p.Asn1805Asp