Canonical Allele Identifier: CA670876328

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1005739087
• MyVariant Identifiers: chr11:g.102669114A>G (hg19) ; chr11:g.102798383A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798383A>G , CM000673.2:g.102798383A>G	GRCh38
NC_000011.9:g.102669114A>G , CM000673.1:g.102669114A>G	GRCh37
NC_000011.8:g.102174324A>G	NCBI36
NG_011740.1:g.4853T>C
NG_011740.2:g.4853T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+261A>G
ENST00000525739.6:n.682+261A>G
ENST00000544704.1:n.443+261A>G
NR_038390.1:n.682+261A>G