Canonical Allele Identifier: CA1956120670
Gene: NAV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547916G= , CM000673.2:g.19547916G= GRCh38
NC_000011.9:g.19569463G= , CM000673.1:g.19569463G= GRCh37
NC_000011.8:g.19526039G= NCBI36
NG_030347.1:g.202193G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+196889G= ENSP00000353871.4:n.75+196889G=
NM_001111018.1:c.75+196889G= NP_001104488.1:n.75+196889G=
XM_011520452.1:c.75+196889G= XP_011518754.1:n.75+196889G=
XM_011520452.2:c.75+196889G= XP_011518754.1:n.75+196889G=
XM_017018520.2:c.75+196889G= XP_016874009.1:n.75+196889G=
XM_017018522.1:c.75+196889G= XP_016874011.1:n.75+196889G=
XM_024448758.1:c.75+196889G= XP_024304526.1:n.75+196889G=
NM_001111018.2:c.75+196889G= NP_001104488.1:n.75+196889G=