Canonical Allele Identifier: CA674422104
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs771982501
gnomAD v3: 11-19547962-G-C
gnomAD v4: 11-19547962-G-C
MyVariant Identifiers: chr11:g.19569509G>C (hg19) chr11:g.19547962G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19547962G>C , CM000673.2:g.19547962G>C GRCh38
NC_000011.9:g.19569509G>C , CM000673.1:g.19569509G>C GRCh37
NC_000011.8:g.19526085G>C NCBI36
NG_030347.1:g.202239G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360655.8:c.75+196935G>C ENSP00000353871.4:n.75+196935G>C
NM_001111018.1:c.75+196935G>C NP_001104488.1:n.75+196935G>C
XM_011520452.1:c.75+196935G>C XP_011518754.1:n.75+196935G>C
XM_011520452.2:c.75+196935G>C XP_011518754.1:n.75+196935G>C
XM_017018520.2:c.75+196935G>C XP_016874009.1:n.75+196935G>C
XM_017018522.1:c.75+196935G>C XP_016874011.1:n.75+196935G>C
XM_024448758.1:c.75+196935G>C XP_024304526.1:n.75+196935G>C
NM_001111018.2:c.75+196935G>C NP_001104488.1:n.75+196935G>C
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