Canonical Allele Identifier: CA65919428
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs766086207
gnomAD v2: 2-219757923-G-T
gnomAD v3: 2-218893201-G-T
gnomAD v4: 2-218893201-G-T
MyVariant Identifiers: chr2:g.219757923G>T (hg19) chr2:g.218893201G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893201G>T , CM000664.2:g.218893201G>T GRCh38
NC_000002.11:g.219757923G>T , CM000664.1:g.219757923G>T GRCh37
NC_000002.10:g.219466167G>T NCBI36
NG_012179.1:g.17669G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1184G>T MANE Select ENSP00000258411.3:p.Arg395Leu
ENST00000258411.7:c.1184G>T ENSP00000258411.3:p.Arg395Leu
NM_025216.2:c.1184G>T NP_079492.2:p.Arg395Leu
XM_011511928.1:c.1133G>T XP_011510230.1:p.Arg378Leu
XM_011511929.1:c.1088G>T XP_011510231.1:p.Arg363Leu
XM_011511930.1:c.804G>T XP_011510232.1:p.Pro268=
XM_011511929.2:c.1088G>T XP_011510231.1:p.Arg363Leu
NM_025216.3:c.1184G>T MANE Select NP_079492.2:p.Arg395Leu
Search 100 bp 5'
Search 100 bp 3'