Canonical Allele Identifier: CA1956120640
Gene: NAV2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547853T= , CM000673.2:g.19547853T= GRCh38
NC_000011.9:g.19569400T= , CM000673.1:g.19569400T= GRCh37
NC_000011.8:g.19525976T= NCBI36
NG_030347.1:g.202130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360655.8:c.75+196826T= ENSP00000353871.4:n.75+196826T=
NM_001111018.1:c.75+196826T= NP_001104488.1:n.75+196826T=
XM_011520452.1:c.75+196826T= XP_011518754.1:n.75+196826T=
XM_011520452.2:c.75+196826T= XP_011518754.1:n.75+196826T=
XM_017018520.2:c.75+196826T= XP_016874009.1:n.75+196826T=
XM_017018522.1:c.75+196826T= XP_016874011.1:n.75+196826T=
XM_024448758.1:c.75+196826T= XP_024304526.1:n.75+196826T=
NM_001111018.2:c.75+196826T= NP_001104488.1:n.75+196826T=
Search 100 bp 5'
Search 100 bp 3'