Canonical Allele Identifier: CA12412569
Gene: MICA HGNC NCBI

Linked Data

dbSNP Id: rs3763288
gnomAD v2: 6-31370367-G-A
gnomAD v3: 6-31402590-G-A
gnomAD v4: 6-31402590-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31402590G>A , CM000668.2:g.31402590G>A GRCh38
NC_000006.11:g.31370367G>A , CM000668.1:g.31370367G>A GRCh37
NC_000006.10:g.31478346G>A NCBI36
NG_034139.1:g.7807G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000667609.1:n.498G>A
ENST00000673647.1:c.-189+234G>A ENSP00000500967.1:n.-189+234G>A
ENST00000673996.1:n.79+1807G>A
ENST00000674069.1:c.-173+1827G>A ENSP00000501157.1:n.-173+1827G>A
ENST00000674131.1:c.-189+234G>A ENSP00000501002.1:n.-189+234G>A
ENST00000616296.4:c.-222+1807G>A ENSP00000482382.1:n.-222+1807G>A
NM_001289152.1:c.-222+1807G>A NP_001276081.1:n.-222+1807G>A
NM_001289153.1:c.-222+1827G>A NP_001276082.1:n.-222+1827G>A
NM_001289154.1:c.-173+1827G>A NP_001276083.1:n.-173+1827G>A
NM_001289152.2:c.-222+1807G>A NP_001276081.1:n.-222+1807G>A
NM_001289153.2:c.-222+1827G>A NP_001276082.1:n.-222+1827G>A
NM_001289154.2:c.-173+1827G>A NP_001276083.1:n.-173+1827G>A