Canonical Allele Identifier: CA1956120736
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs2044562852

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548064T>G , CM000673.2:g.19548064T>G GRCh38
NC_000011.9:g.19569611T>G , CM000673.1:g.19569611T>G GRCh37
NC_000011.8:g.19526187T>G NCBI36
NG_030347.1:g.202341T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+197037T>G ENSP00000353871.4:n.75+197037T>G
NM_001111018.1:c.75+197037T>G NP_001104488.1:n.75+197037T>G
XM_011520452.1:c.75+197037T>G XP_011518754.1:n.75+197037T>G
XM_011520452.2:c.75+197037T>G XP_011518754.1:n.75+197037T>G
XM_017018520.2:c.75+197037T>G XP_016874009.1:n.75+197037T>G
XM_017018522.1:c.75+197037T>G XP_016874011.1:n.75+197037T>G
XM_024448758.1:c.75+197037T>G XP_024304526.1:n.75+197037T>G
NM_001111018.2:c.75+197037T>G NP_001104488.1:n.75+197037T>G