Canonical Allele Identifier: CA1956120688
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs2044558145

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547971C>T , CM000673.2:g.19547971C>T GRCh38
NC_000011.9:g.19569518C>T , CM000673.1:g.19569518C>T GRCh37
NC_000011.8:g.19526094C>T NCBI36
NG_030347.1:g.202248C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+196944C>T ENSP00000353871.4:n.75+196944C>T
NM_001111018.1:c.75+196944C>T NP_001104488.1:n.75+196944C>T
XM_011520452.1:c.75+196944C>T XP_011518754.1:n.75+196944C>T
XM_011520452.2:c.75+196944C>T XP_011518754.1:n.75+196944C>T
XM_017018520.2:c.75+196944C>T XP_016874009.1:n.75+196944C>T
XM_017018522.1:c.75+196944C>T XP_016874011.1:n.75+196944C>T
XM_024448758.1:c.75+196944C>T XP_024304526.1:n.75+196944C>T
NM_001111018.2:c.75+196944C>T NP_001104488.1:n.75+196944C>T