Canonical Allele Identifier: CA28632622
Gene: CELSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1035966774

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264355G>T , CM000663.2:g.109264355G>T GRCh38
NC_000001.10:g.109806977G>T , CM000663.1:g.109806977G>T GRCh37
NC_000001.9:g.109608500G>T NCBI36
NG_052669.1:g.19651G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5279G>T MANE Select ENSP00000271332.3:p.Gly1760Val
ENST00000271332.3:c.5279G>T ENSP00000271332.3:p.Gly1760Val
NM_001408.2:c.5279G>T NP_001399.1:p.Gly1760Val
XM_005270580.3:c.5279G>T XP_005270637.1:p.Gly1760Val
NM_001408.3:c.5279G>T MANE Select NP_001399.1:p.Gly1760Val