Canonical Allele Identifier: CA670876376

Gene: WTAPP1

Linked Data

• dbSNP Id: rs1297137109
• MyVariant Identifiers: chr11:g.102669183G>T (hg19) ; chr11:g.102798452G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102798452G>T , CM000673.2:g.102798452G>T	GRCh38
NC_000011.9:g.102669183G>T , CM000673.1:g.102669183G>T	GRCh37
NC_000011.8:g.102174393G>T	NCBI36
NG_011740.1:g.4784C>A
NG_011740.2:g.4784C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371455.7:n.423+330G>T
ENST00000525739.6:n.682+330G>T
ENST00000544704.1:n.443+330G>T
NR_038390.1:n.682+330G>T