Canonical Allele Identifier: CA1188034928
Gene: CELSR2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264073G= , CM000663.2:g.109264073G= GRCh38
NC_000001.10:g.109806695G= , CM000663.1:g.109806695G= GRCh37
NC_000001.9:g.109608218G= NCBI36
NG_052669.1:g.19369G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5002-5G= MANE Select ENSP00000271332.3:n.5002-5G=
ENST00000271332.3:c.5002-5G= ENSP00000271332.3:n.5002-5G=
NM_001408.2:c.5002-5G= NP_001399.1:n.5002-5G=
XM_005270580.3:c.5002-5G= XP_005270637.1:n.5002-5G=
NM_001408.3:c.5002-5G= MANE Select NP_001399.1:n.5002-5G=
Search 100 bp 5'
Search 100 bp 3'