Canonical Allele Identifier: CA1956120661
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs2044555731

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547890G>T , CM000673.2:g.19547890G>T GRCh38
NC_000011.9:g.19569437G>T , CM000673.1:g.19569437G>T GRCh37
NC_000011.8:g.19526013G>T NCBI36
NG_030347.1:g.202167G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360655.8:c.75+196863G>T ENSP00000353871.4:n.75+196863G>T
NM_001111018.1:c.75+196863G>T NP_001104488.1:n.75+196863G>T
XM_011520452.1:c.75+196863G>T XP_011518754.1:n.75+196863G>T
XM_011520452.2:c.75+196863G>T XP_011518754.1:n.75+196863G>T
XM_017018520.2:c.75+196863G>T XP_016874009.1:n.75+196863G>T
XM_017018522.1:c.75+196863G>T XP_016874011.1:n.75+196863G>T
XM_024448758.1:c.75+196863G>T XP_024304526.1:n.75+196863G>T
NM_001111018.2:c.75+196863G>T NP_001104488.1:n.75+196863G>T