Canonical Allele Identifier: CA341502147
Gene: CELSR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264551C>G , CM000663.2:g.109264551C>G GRCh38
NC_000001.10:g.109807173C>G , CM000663.1:g.109807173C>G GRCh37
NC_000001.9:g.109608696C>G NCBI36
NG_052669.1:g.19847C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5387C>G MANE Select ENSP00000271332.3:p.Pro1796Arg
ENST00000271332.3:c.5387C>G ENSP00000271332.3:p.Pro1796Arg
NM_001408.2:c.5387C>G NP_001399.1:p.Pro1796Arg
XM_005270580.3:c.5387C>G XP_005270637.1:p.Pro1796Arg
NM_001408.3:c.5387C>G MANE Select NP_001399.1:p.Pro1796Arg