Canonical Allele Identifier: CA419677908
Gene: CELSR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.109806729G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109264107G>A , CM000663.2:g.109264107G>A GRCh38
NC_000001.10:g.109806729G>A , CM000663.1:g.109806729G>A GRCh37
NC_000001.9:g.109608252G>A NCBI36
NG_052669.1:g.19403G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271332.4:c.5031G>A MANE Select ENSP00000271332.3:p.Val1677=
ENST00000271332.3:c.5031G>A ENSP00000271332.3:p.Val1677=
NM_001408.2:c.5031G>A NP_001399.1:p.Val1677=
XM_005270580.3:c.5031G>A XP_005270637.1:p.Val1677=
NM_001408.3:c.5031G>A MANE Select NP_001399.1:p.Val1677=
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