Canonical Allele Identifier: CA1188034939
Gene: CELSR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264095G= , CM000663.2:g.109264095G= GRCh38
NC_000001.10:g.109806717G= , CM000663.1:g.109806717G= GRCh37
NC_000001.9:g.109608240G= NCBI36
NG_052669.1:g.19391G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5019G= MANE Select ENSP00000271332.3:p.Val1673=
ENST00000271332.3:c.5019G= ENSP00000271332.3:p.Val1673=
NM_001408.2:c.5019G= NP_001399.1:p.Val1673=
XM_005270580.3:c.5019G= XP_005270637.1:p.Val1673=
NM_001408.3:c.5019G= MANE Select NP_001399.1:p.Val1673=
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