Canonical Allele Identifier: CA329506641
Gene: EFHC2 HGNC NCBI

Linked Data

dbSNP Id: rs7055196
gnomAD v2: X-44104538-A-G
gnomAD v3: X-44245292-A-G
gnomAD v4: X-44245292-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44245292A>G , CM000685.2:g.44245292A>G GRCh38
NC_000023.10:g.44104538A>G , CM000685.1:g.44104538A>G GRCh37
NC_000023.9:g.43989482A>G NCBI36
NG_021391.1:g.103387T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420999.2:c.1111+2980T>C MANE Select ENSP00000404232.2:n.1111+2980T>C
ENST00000420999.1:c.1111+2980T>C ENSP00000404232.2:n.1111+2980T>C
NM_025184.3:c.1111+2980T>C NP_079460.2:n.1111+2980T>C
XM_005272671.2:c.1111+2980T>C XP_005272728.1:n.1111+2980T>C
XM_006724562.2:c.523+2980T>C XP_006724625.1:n.523+2980T>C
XR_949019.1:n.1188+2980T>C
XM_024452453.1:c.1015+2980T>C XP_024308221.1:n.1015+2980T>C
NM_025184.4:c.1111+2980T>C MANE Select NP_079460.2:n.1111+2980T>C