Canonical Allele Identifier: CA2202666018
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3256628T= , CM000678.2:g.3256628T= GRCh38
NC_000016.9:g.3306628T= , CM000678.1:g.3306628T= GRCh37
NC_000016.8:g.3246629T= NCBI36
NG_007871.1:g.5000A= , LRG_190:g.5000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.-41A= MANE Select ENSP00000219596.1:n.-41A=
XM_017023236.2:c.-41A= XP_016878725.1:n.-41A=
XR_001751903.1:n.149A=
NM_000243.3:c.-41A= MANE Select NP_000234.1:n.-41A=
NM_001198536.2:c.-41A= NP_001185465.2:n.-41A=