Canonical Allele Identifier: CA597520176

Gene: NAV2

Linked Data

• dbSNP Id: rs1371797567
• gnomAD v2: 11-19569810-A-C
• gnomAD v3: 11-19548263-A-C
• gnomAD v4: 11-19548263-A-C
• MyVariant Identifiers: chr11:g.19569810A>C (hg19) ; chr11:g.19548263A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19548263A>C , CM000673.2:g.19548263A>C	GRCh38
NC_000011.9:g.19569810A>C , CM000673.1:g.19569810A>C	GRCh37
NC_000011.8:g.19526386A>C	NCBI36
NG_030347.1:g.202540A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360655.8:c.75+197236A>C	ENSP00000353871.4:n.75+197236A>C
NM_001111018.1:c.75+197236A>C	NP_001104488.1:n.75+197236A>C
XM_011520452.1:c.75+197236A>C	XP_011518754.1:n.75+197236A>C
XM_011520452.2:c.75+197236A>C	XP_011518754.1:n.75+197236A>C
XM_017018520.2:c.75+197236A>C	XP_016874009.1:n.75+197236A>C
XM_017018522.1:c.75+197236A>C	XP_016874011.1:n.75+197236A>C
XM_024448758.1:c.75+197236A>C	XP_024304526.1:n.75+197236A>C
NM_001111018.2:c.75+197236A>C	NP_001104488.1:n.75+197236A>C