Canonical Allele Identifier: CA28631996

Gene: CELSR2

Linked Data

• dbSNP Id: rs56197083
• gnomAD v2: 1-109806550-G-T
• gnomAD v3: 1-109263928-G-T
• gnomAD v4: 1-109263928-G-T
• MyVariant Identifiers: chr1:g.109806550G>T (hg19) ; chr1:g.109263928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109263928G>T , CM000663.2:g.109263928G>T	GRCh38
NC_000001.10:g.109806550G>T , CM000663.1:g.109806550G>T	GRCh37
NC_000001.9:g.109608073G>T	NCBI36
NG_052669.1:g.19224G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271332.4:c.5002-150G>T MANE Select	ENSP00000271332.3:n.5002-150G>T
ENST00000271332.3:c.5002-150G>T	ENSP00000271332.3:n.5002-150G>T
NM_001408.2:c.5002-150G>T	NP_001399.1:n.5002-150G>T
XM_005270580.3:c.5002-150G>T	XP_005270637.1:n.5002-150G>T
NM_001408.3:c.5002-150G>T MANE Select	NP_001399.1:n.5002-150G>T