Canonical Allele Identifier: CA2202666020
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3256630G= , CM000678.2:g.3256630G= GRCh38
NC_000016.9:g.3306630G= , CM000678.1:g.3306630G= GRCh37
NC_000016.8:g.3246631G= NCBI36
NG_007871.1:g.4998C= , LRG_190:g.4998C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.-43C= MANE Select ENSP00000219596.1:n.-43C=
XM_017023236.2:c.-43C= XP_016878725.1:n.-43C=
XR_001751903.1:n.147C=
NM_000243.3:c.-43C= MANE Select NP_000234.1:n.-43C=
NM_001198536.2:c.-43C= NP_001185465.2:n.-43C=