Canonical Allele Identifier: CA15250161
Gene: MME HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1836915

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.155091313T>C , CM000665.2:g.155091313T>C GRCh38
NC_000003.11:g.154809102T>C , CM000665.1:g.154809102T>C GRCh37
NC_000003.10:g.156291796T>C NCBI36
NG_051105.1:g.72190T>C

Transcript Alleles

HGVS Amino-acid change
NM_000902.3:c.196+6219T>C VV NP_000893.2:p.=
NM_007287.2:c.196+6219T>C VV NP_009218.2:p.=
NM_007288.2:c.196+6219T>C VV NP_009219.2:p.=
NM_007289.2:c.196+6219T>C VV NP_009220.2:p.=
XM_006713646.2:c.196+6219T>C XP_006713709.1:p.=
XM_006713647.2:c.196+6219T>C XP_006713710.1:p.=
XM_011512855.1:c.196+6219T>C XP_011511157.1:p.=
XM_011512856.1:c.196+6219T>C XP_011511158.1:p.=
XM_011512857.1:c.196+6219T>C XP_011511159.1:p.=
XM_011512858.1:c.196+6219T>C XP_011511160.1:p.=
NM_001354642.1:c.196+6219T>C VV NP_001341571.1:p.=
NM_001354643.1:c.196+6219T>C VV NP_001341572.1:p.=
NM_007288.3:c.196+6219T>C VV NP_009219.2:p.=
NM_007289.3:c.196+6219T>C VV NP_009220.2:p.=
XM_006713647.4:c.196+6219T>C XP_006713710.1:p.=
XM_011512856.2:c.196+6219T>C XP_011511158.1:p.=
XM_011512857.2:c.196+6219T>C XP_011511159.1:p.=
ENST00000360490.6:c.196+6219T>C ENSP00000353679.2:p.=
ENST00000460393.5:c.196+6219T>C ENSP00000418525.1:p.=
ENST00000462745.5:c.196+6219T>C ENSP00000419653.1:p.=
ENST00000462837.5:c.196+6219T>C ENSP00000417595.1:p.=
ENST00000473730.5:c.196+6219T>C ENSP00000420542.1:p.=
ENST00000481828.5:c.196+6219T>C ENSP00000420101.1:p.=
ENST00000491026.5:c.196+6219T>C ENSP00000418791.1:p.=
ENST00000492661.5:c.196+6219T>C ENSP00000420389.1:p.=
ENST00000493237.5:c.196+6219T>C ENSP00000417079.1:p.=
ENST00000615825.1:n.196+6219T>C ENSP00000478173.1:p.=