Canonical Allele Identifier: CA449643584

Gene: MICA

Linked Data

• dbSNP Id: rs1770467973
• MyVariant Identifiers: chr6:g.31369977T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31402200T>C , CM000668.2:g.31402200T>C	GRCh38
NC_000006.11:g.31369977T>C , CM000668.1:g.31369977T>C	GRCh37
NC_000006.10:g.31477956T>C	NCBI36
NG_034139.1:g.7417T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000667609.1:n.108T>C
ENST00000673647.1:c.-345T>C	ENSP00000500967.1:n.-345T>C
ENST00000673996.1:n.79+1417T>C
ENST00000674069.1:c.-173+1437T>C	ENSP00000501157.1:n.-173+1437T>C
ENST00000674131.1:c.-345T>C	ENSP00000501002.1:n.-345T>C
ENST00000616296.4:c.-222+1417T>C	ENSP00000482382.1:n.-222+1417T>C
NM_001289152.1:c.-222+1417T>C	NP_001276081.1:n.-222+1417T>C
NM_001289153.1:c.-222+1437T>C	NP_001276082.1:n.-222+1437T>C
NM_001289154.1:c.-173+1437T>C	NP_001276083.1:n.-173+1437T>C
NM_001289152.2:c.-222+1417T>C	NP_001276081.1:n.-222+1417T>C
NM_001289153.2:c.-222+1437T>C	NP_001276082.1:n.-222+1437T>C
NM_001289154.2:c.-173+1437T>C	NP_001276083.1:n.-173+1437T>C