Canonical Allele Identifier: CA674422248
Gene: NAV2 HGNC NCBI

Linked Data

dbSNP Id: rs1192605369
MyVariant Identifiers: chr11:g.19569706G>A (hg19) chr11:g.19548159G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19548159G>A , CM000673.2:g.19548159G>A GRCh38
NC_000011.9:g.19569706G>A , CM000673.1:g.19569706G>A GRCh37
NC_000011.8:g.19526282G>A NCBI36
NG_030347.1:g.202436G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360655.8:c.75+197132G>A ENSP00000353871.4:n.75+197132G>A
NM_001111018.1:c.75+197132G>A NP_001104488.1:n.75+197132G>A
XM_011520452.1:c.75+197132G>A XP_011518754.1:n.75+197132G>A
XM_011520452.2:c.75+197132G>A XP_011518754.1:n.75+197132G>A
XM_017018520.2:c.75+197132G>A XP_016874009.1:n.75+197132G>A
XM_017018522.1:c.75+197132G>A XP_016874011.1:n.75+197132G>A
XM_024448758.1:c.75+197132G>A XP_024304526.1:n.75+197132G>A
NM_001111018.2:c.75+197132G>A NP_001104488.1:n.75+197132G>A
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