Canonical Allele Identifier: CA218812545

Gene: NAV2

Linked Data

• dbSNP Id: rs953481165
• MyVariant Identifiers: chr11:g.19569582A>G (hg19) ; chr11:g.19548035A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19548035A>G , CM000673.2:g.19548035A>G	GRCh38
NC_000011.9:g.19569582A>G , CM000673.1:g.19569582A>G	GRCh37
NC_000011.8:g.19526158A>G	NCBI36
NG_030347.1:g.202312A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360655.8:c.75+197008A>G	ENSP00000353871.4:n.75+197008A>G
NM_001111018.1:c.75+197008A>G	NP_001104488.1:n.75+197008A>G
XM_011520452.1:c.75+197008A>G	XP_011518754.1:n.75+197008A>G
XM_011520452.2:c.75+197008A>G	XP_011518754.1:n.75+197008A>G
XM_017018520.2:c.75+197008A>G	XP_016874009.1:n.75+197008A>G
XM_017018522.1:c.75+197008A>G	XP_016874011.1:n.75+197008A>G
XM_024448758.1:c.75+197008A>G	XP_024304526.1:n.75+197008A>G
NM_001111018.2:c.75+197008A>G	NP_001104488.1:n.75+197008A>G