Canonical Allele Identifier: CA2202666019
Gene: MEFV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3256629G= , CM000678.2:g.3256629G= GRCh38
NC_000016.9:g.3306629G= , CM000678.1:g.3306629G= GRCh37
NC_000016.8:g.3246630G= NCBI36
NG_007871.1:g.4999C= , LRG_190:g.4999C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219596.6:c.-42C= MANE Select ENSP00000219596.1:n.-42C=
XM_017023236.2:c.-42C= XP_016878725.1:n.-42C=
XR_001751903.1:n.148C=
NM_000243.3:c.-42C= MANE Select NP_000234.1:n.-42C=
NM_001198536.2:c.-42C= NP_001185465.2:n.-42C=