Canonical Allele Identifier: CA341501933
Gene: CELSR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.109807075G>C (hg19) chr1:g.109264453G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264453G>C , CM000663.2:g.109264453G>C GRCh38
NC_000001.10:g.109807075G>C , CM000663.1:g.109807075G>C GRCh37
NC_000001.9:g.109608598G>C NCBI36
NG_052669.1:g.19749G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5290-1G>C MANE Select ENSP00000271332.3:n.5290-1G>C
ENST00000271332.3:c.5290-1G>C ENSP00000271332.3:n.5290-1G>C
NM_001408.2:c.5290-1G>C NP_001399.1:n.5290-1G>C
XM_005270580.3:c.5290-1G>C XP_005270637.1:n.5290-1G>C
NM_001408.3:c.5290-1G>C MANE Select NP_001399.1:n.5290-1G>C
Search 100 bp 5'
Search 100 bp 3'