Canonical Allele Identifier: CA218812515

Gene: NAV2

Linked Data

• dbSNP Id: rs776284363
• gnomAD v3: 11-19547759-C-CA
• gnomAD v4: 11-19547759-C-CA
• MyVariant Identifiers: chr11:g.19569306_19569307insA (hg19) ; chr11:g.19547759_19547760insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19547761dup , CM000673.2:g.19547761dup	GRCh38
NC_000011.9:g.19569308dup , CM000673.1:g.19569308dup	GRCh37
NC_000011.8:g.19525884dup	NCBI36
NG_030347.1:g.202038dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360655.8:c.75+196734dup	ENSP00000353871.4:n.75+196734dup
NM_001111018.1:c.75+196734dup	NP_001104488.1:n.75+196734dup
XM_011520452.1:c.75+196734dup	XP_011518754.1:n.75+196734dup
XM_011520452.2:c.75+196734dup	XP_011518754.1:n.75+196734dup
XM_017018520.2:c.75+196734dup	XP_016874009.1:n.75+196734dup
XM_017018522.1:c.75+196734dup	XP_016874011.1:n.75+196734dup
XM_024448758.1:c.75+196734dup	XP_024304526.1:n.75+196734dup
NM_001111018.2:c.75+196734dup	NP_001104488.1:n.75+196734dup