Canonical Allele Identifier: CA1956120737
Gene: NAV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548066A= , CM000673.2:g.19548066A= GRCh38
NC_000011.9:g.19569613A= , CM000673.1:g.19569613A= GRCh37
NC_000011.8:g.19526189A= NCBI36
NG_030347.1:g.202343A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+197039A= ENSP00000353871.4:n.75+197039A=
NM_001111018.1:c.75+197039A= NP_001104488.1:n.75+197039A=
XM_011520452.1:c.75+197039A= XP_011518754.1:n.75+197039A=
XM_011520452.2:c.75+197039A= XP_011518754.1:n.75+197039A=
XM_017018520.2:c.75+197039A= XP_016874009.1:n.75+197039A=
XM_017018522.1:c.75+197039A= XP_016874011.1:n.75+197039A=
XM_024448758.1:c.75+197039A= XP_024304526.1:n.75+197039A=
NM_001111018.2:c.75+197039A= NP_001104488.1:n.75+197039A=