Canonical Allele Identifier: CA13138422
Gene: DIP2C HGNC NCBI

Linked Data

dbSNP Id: rs17221323
gnomAD v2: 10-618685-T-C
gnomAD v3: 10-572745-T-C
gnomAD v4: 10-572745-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.572745T>C , CM000672.2:g.572745T>C GRCh38
NC_000010.10:g.618685T>C , CM000672.1:g.618685T>C GRCh37
NC_000010.9:g.608685T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000280886.12:c.86-86215A>G MANE Select ENSP00000280886.6:n.86-86215A>G
ENST00000280886.11:c.86-86215A>G ENSP00000280886.6:n.86-86215A>G
ENST00000634311.1:c.86-86215A>G ENSP00000489203.1:n.86-86215A>G
NM_014974.2:c.86-86215A>G NP_055789.1:n.86-86215A>G
XM_005252426.2:c.86-86215A>G XP_005252483.1:n.86-86215A>G
XM_005252427.2:c.86-86215A>G XP_005252484.1:n.86-86215A>G
XM_005252428.3:c.86-86215A>G XP_005252485.1:n.86-86215A>G
XM_011519432.1:c.-236-86215A>G XP_011517734.1:n.-236-86215A>G
XM_005252426.3:c.86-86215A>G XP_005252483.1:n.86-86215A>G
XM_005252427.4:c.86-86215A>G XP_005252484.1:n.86-86215A>G
XM_005252428.4:c.86-86215A>G XP_005252485.1:n.86-86215A>G
XM_011519432.2:c.-236-86215A>G XP_011517734.1:n.-236-86215A>G
NM_014974.3:c.86-86215A>G MANE Select NP_055789.1:n.86-86215A>G