Canonical Allele Identifier: CA341501995
Gene: CELSR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.109807107T>A (hg19) chr1:g.109264485T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264485T>A , CM000663.2:g.109264485T>A GRCh38
NC_000001.10:g.109807107T>A , CM000663.1:g.109807107T>A GRCh37
NC_000001.9:g.109608630T>A NCBI36
NG_052669.1:g.19781T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5321T>A MANE Select ENSP00000271332.3:p.Val1774Asp
ENST00000271332.3:c.5321T>A ENSP00000271332.3:p.Val1774Asp
NM_001408.2:c.5321T>A NP_001399.1:p.Val1774Asp
XM_005270580.3:c.5321T>A XP_005270637.1:p.Val1774Asp
NM_001408.3:c.5321T>A MANE Select NP_001399.1:p.Val1774Asp
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