Canonical Allele Identifier: CA1956120691
Gene: NAV2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547983C= , CM000673.2:g.19547983C= GRCh38
NC_000011.9:g.19569530C= , CM000673.1:g.19569530C= GRCh37
NC_000011.8:g.19526106C= NCBI36
NG_030347.1:g.202260C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360655.8:c.75+196956C= ENSP00000353871.4:n.75+196956C=
NM_001111018.1:c.75+196956C= NP_001104488.1:n.75+196956C=
XM_011520452.1:c.75+196956C= XP_011518754.1:n.75+196956C=
XM_011520452.2:c.75+196956C= XP_011518754.1:n.75+196956C=
XM_017018520.2:c.75+196956C= XP_016874009.1:n.75+196956C=
XM_017018522.1:c.75+196956C= XP_016874011.1:n.75+196956C=
XM_024448758.1:c.75+196956C= XP_024304526.1:n.75+196956C=
NM_001111018.2:c.75+196956C= NP_001104488.1:n.75+196956C=
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