Canonical Allele Identifier: CA2039024935
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI

Linked Data

dbSNP Id: rs1595098416
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739459T>C , CM000674.2:g.57739459T>C GRCh38
NC_000012.11:g.58133242T>C , CM000674.1:g.58133242T>C GRCh37
NC_000012.10:g.56419509T>C NCBI36
NG_029755.1:g.7703A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000257897.7:c.160+2453A>G (AGAP2) ENSP00000257897.3:n.160+2453A>G
ENST00000553221.5:n.189+1258T>C (TSPAN31)
NM_014770.3:c.160+2453A>G (AGAP2) NP_055585.1:n.160+2453A>G
XM_005268626.1:c.160+2453A>G (AGAP2) XP_005268683.1:n.160+2453A>G
XM_005268626.2:c.160+2453A>G (AGAP2) XP_005268683.1:n.160+2453A>G
NM_014770.4:c.160+2453A>G (AGAP2) NP_055585.1:n.160+2453A>G
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