Canonical Allele Identifier: CA419678590

Gene: CELSR2

Linked Data

• MyVariant Identifiers: chr1:g.109806978C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109264356C>T , CM000663.2:g.109264356C>T	GRCh38
NC_000001.10:g.109806978C>T , CM000663.1:g.109806978C>T	GRCh37
NC_000001.9:g.109608501C>T	NCBI36
NG_052669.1:g.19652C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5280C>T MANE Select	ENSP00000271332.3:p.Gly1760=
ENST00000271332.3:c.5280C>T	ENSP00000271332.3:p.Gly1760=
NM_001408.2:c.5280C>T	NP_001399.1:p.Gly1760=
XM_005270580.3:c.5280C>T	XP_005270637.1:p.Gly1760=
NM_001408.3:c.5280C>T MANE Select	NP_001399.1:p.Gly1760=