Canonical Allele Identifier: CA1956030178

Gene: NAV2

Linked Data

• dbSNP Id: rs1853396312

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19352741_19352743del , CM000673.2:g.19352741_19352743del	GRCh38
NC_000011.9:g.19374288_19374290del , CM000673.1:g.19374288_19374290del	GRCh37
NC_000011.8:g.19330864_19330866del	NCBI36
NG_030347.1:g.7018_7020del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360655.8:c.75+1714_75+1716del	ENSP00000353871.4:n.75+1714_75+1716del
NM_001111018.1:c.75+1714_75+1716del	NP_001104488.1:n.75+1714_75+1716del
XM_011520452.1:c.75+1714_75+1716del	XP_011518754.1:n.75+1714_75+1716del
XM_011520452.2:c.75+1714_75+1716del	XP_011518754.1:n.75+1714_75+1716del
XM_017018520.2:c.75+1714_75+1716del	XP_016874009.1:n.75+1714_75+1716del
XM_017018522.1:c.75+1714_75+1716del	XP_016874011.1:n.75+1714_75+1716del
XM_024448758.1:c.75+1714_75+1716del	XP_024304526.1:n.75+1714_75+1716del
NM_001111018.2:c.75+1714_75+1716del	NP_001104488.1:n.75+1714_75+1716del