Canonical Allele Identifier: CA493384193
Gene: MEFV HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3304537G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3254537G>A , CM000678.2:g.3254537G>A GRCh38
NC_000016.9:g.3304537G>A , CM000678.1:g.3304537G>A GRCh37
NC_000016.8:g.3244538G>A NCBI36
NG_007871.1:g.7091C>T , LRG_190:g.7091C>T

Transcript Alleles

HGVS Amino-acid change
NM_000243.2:c.531C>T , LRG_190t1:c.531C>T NP_000234.1:p.Thr177=
NM_001198536.1:c.277+1774C>T NP_001185465.1:p.=
XM_017023236.2:c.531C>T XP_016878725.1:p.Thr177=
XR_001751903.1:n.720C>T
NM_000243.3:c.531C>T MANE Select NP_000234.1:p.Thr177=
NM_001198536.2:c.277+1774C>T NP_001185465.2:p.=
ENST00000219596.5:c.531C>T ENSP00000219596.1:p.Thr177=
ENST00000339854.8:c.277+1774C>T ENSP00000339639.4:p.=
ENST00000536379.5:n.277+1774C>T ENSP00000445079.1:p.=
ENST00000536980.5:c.277+1774C>T ENSP00000444178.1:p.=
ENST00000537682.5:c.531C>T ENSP00000438611.1:p.Thr177=
ENST00000538326.5:c.531C>T ENSP00000437486.1:p.Thr177=
ENST00000539145.5:n.277+1774C>T ENSP00000444471.1:p.=
ENST00000541159.5:n.277+1774C>T ENSP00000438711.1:p.=
ENST00000542898.5:c.531C>T ENSP00000444615.1:p.Thr177=
ENST00000570511.5:n.531C>T ENSP00000458312.1:p.Thr177=
ENST00000572244.5:n.277+1774C>T ENSP00000461186.1:p.=
ENST00000574583.5:n.277+1774C>T ENSP00000460269.1:p.=
ENST00000576315.5:n.277+1774C>T ENSP00000460551.1:p.=
ENST00000621655.1:n.277+1774C>T ENSP00000481436.1:p.=