Canonical Allele Identifier: CA935674036
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs2044562141

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548040G>C , CM000673.2:g.19548040G>C GRCh38
NC_000011.9:g.19569587G>C , CM000673.1:g.19569587G>C GRCh37
NC_000011.8:g.19526163G>C NCBI36
NG_030347.1:g.202317G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+197013G>C ENSP00000353871.4:n.75+197013G>C
NM_001111018.1:c.75+197013G>C NP_001104488.1:n.75+197013G>C
XM_011520452.1:c.75+197013G>C XP_011518754.1:n.75+197013G>C
XM_011520452.2:c.75+197013G>C XP_011518754.1:n.75+197013G>C
XM_017018520.2:c.75+197013G>C XP_016874009.1:n.75+197013G>C
XM_017018522.1:c.75+197013G>C XP_016874011.1:n.75+197013G>C
XM_024448758.1:c.75+197013G>C XP_024304526.1:n.75+197013G>C
NM_001111018.2:c.75+197013G>C NP_001104488.1:n.75+197013G>C