Canonical Allele Identifier: CA91734645
Gene: EVC HGNC NCBI

Linked Data

dbSNP Id: rs894280517
gnomAD v3: 4-5711199-C-T
gnomAD v4: 4-5711199-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5711199C>T , CM000666.2:g.5711199C>T GRCh38
NC_000004.11:g.5712926C>T , CM000666.1:g.5712926C>T GRCh37
NC_000004.10:g.5763827C>T NCBI36
NG_008843.1:g.5003C>T
NG_015821.1:g.3350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264956.10:c.-182C>T ENSP00000264956.6:n.-182C>T
NM_001306090.1:c.-182C>T NP_001293019.1:n.-182C>T
NM_001306092.1:c.-182C>T NP_001293021.1:n.-182C>T
NM_153717.2:c.-182C>T NP_714928.1:n.-182C>T
XM_006713865.2:c.-182C>T XP_006713928.1:n.-182C>T
XM_006713866.2:c.-182C>T XP_006713929.1:n.-182C>T
XM_011513419.1:c.-182C>T XP_011511721.1:n.-182C>T
XR_427473.2:n.9C>T
XR_427475.2:n.9C>T
XR_427476.2:n.9C>T
XR_924920.1:n.9C>T
XR_924921.1:n.9C>T
XR_924922.1:n.9C>T
XR_924923.1:n.9C>T
XR_924924.1:n.9C>T
XR_924925.1:n.9C>T
XR_924926.1:n.9C>T
XR_924927.1:n.9C>T
XR_924928.1:n.11C>T
XR_001741169.2:n.1C>T
XR_001741170.1:n.1C>T