Canonical Allele Identifier: CA15446389
Gene: MICB HGNC NCBI

Linked Data

dbSNP Id: rs2855804
gnomAD v2: 6-31467365-C-T
gnomAD v3: 6-31499588-C-T
gnomAD v4: 6-31499588-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31499588C>T , CM000668.2:g.31499588C>T GRCh38
NC_000006.11:g.31467365C>T , CM000668.1:g.31467365C>T GRCh37
NC_000006.10:g.31575344C>T NCBI36
NG_021405.1:g.6511C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252229.7:c.70+1325C>T MANE Select ENSP00000252229.6:n.70+1325C>T
ENST00000252229.6:c.70+1325C>T ENSP00000252229.6:n.70+1325C>T
ENST00000399150.7:c.70+1325C>T ENSP00000382103.3:n.70+1325C>T
ENST00000538442.5:c.-27+4593C>T ENSP00000442345.1:n.-27+4593C>T
NM_001289160.1:c.-27+4593C>T NP_001276089.1:n.-27+4593C>T
NM_001289161.1:c.70+1325C>T NP_001276090.1:n.70+1325C>T
NM_005931.4:c.70+1325C>T NP_005922.2:n.70+1325C>T
XM_011514630.1:c.-27+4612C>T XP_011512932.1:n.-27+4612C>T
XM_011514631.1:c.-27+2688C>T XP_011512933.1:n.-27+2688C>T
NM_005931.5:c.70+1325C>T MANE Select NP_005922.2:n.70+1325C>T
NM_001289161.2:c.70+1325C>T NP_001276090.1:n.70+1325C>T
NM_001289160.2:c.-27+4593C>T NP_001276089.1:n.-27+4593C>T