Canonical Allele Identifier: CA1619182306
Gene: MICB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31496962G= , CM000668.2:g.31496962G= GRCh38
NC_000006.11:g.31464739G= , CM000668.1:g.31464739G= GRCh37
NC_000006.10:g.31572718G= NCBI36
NG_021405.1:g.3885G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000538442.5:c.-27+1967G= ENSP00000442345.1:n.-27+1967G=
NM_001289160.1:c.-27+1967G= NP_001276089.1:n.-27+1967G=
XM_011514630.1:c.-27+1986G= XP_011512932.1:n.-27+1986G=
XM_011514631.1:c.-27+62G= XP_011512933.1:n.-27+62G=
NM_001289160.2:c.-27+1967G= NP_001276089.1:n.-27+1967G=