Canonical Allele Identifier: CA356147876
Gene: EVC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5628702C>A , CM000666.2:g.5628702C>A GRCh38
NC_000004.11:g.5630429C>A , CM000666.1:g.5630429C>A GRCh37
NC_000004.10:g.5681330C>A NCBI36
NG_015821.1:g.85847G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344408.10:c.1743G>T MANE Select ENSP00000342144.5:p.Gln581His
ENST00000310917.6:c.1503G>T ENSP00000311683.2:p.Gln501His
ENST00000344408.9:c.1743G>T ENSP00000342144.5:p.Gln581His
ENST00000475313.5:c.1503G>T ENSP00000431981.1:p.Gln501His
ENST00000509670.1:c.*136G>T ENSP00000423876.1:n.*136G>T
NM_001166136.1:c.1503G>T NP_001159608.1:p.Gln501His
NM_147127.4:c.1743G>T NP_667338.3:p.Gln581His
XM_011513392.1:c.1752G>T XP_011511694.1:p.Gln584His
XM_011513393.1:c.1752G>T XP_011511695.1:p.Gln584His
XM_011513394.1:c.1512G>T XP_011511696.1:p.Gln504His
XM_017007736.1:c.1503G>T XP_016863225.1:p.Gln501His
XM_017007737.1:c.1503G>T XP_016863226.1:p.Gln501His
XM_017007738.1:c.1743G>T XP_016863227.1:p.Gln581His
XM_017007739.1:c.63G>T XP_016863228.1:p.Gln21His
XM_024453893.1:c.63G>T XP_024309661.1:p.Gln21His
XR_001741141.1:n.1808G>T
NM_147127.5:c.1743G>T MANE Select NP_667338.3:p.Gln581His
NM_001166136.2:c.1503G>T NP_001159608.1:p.Gln501His