Canonical Allele Identifier: CA935674038
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs2044562485

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548061del , CM000673.2:g.19548061del GRCh38
NC_000011.9:g.19569608del , CM000673.1:g.19569608del GRCh37
NC_000011.8:g.19526184del NCBI36
NG_030347.1:g.202338del

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+197034del ENSP00000353871.4:n.75+197034del
NM_001111018.1:c.75+197034del NP_001104488.1:n.75+197034del
XM_011520452.1:c.75+197034del XP_011518754.1:n.75+197034del
XM_011520452.2:c.75+197034del XP_011518754.1:n.75+197034del
XM_017018520.2:c.75+197034del XP_016874009.1:n.75+197034del
XM_017018522.1:c.75+197034del XP_016874011.1:n.75+197034del
XM_024448758.1:c.75+197034del XP_024304526.1:n.75+197034del
NM_001111018.2:c.75+197034del NP_001104488.1:n.75+197034del