Canonical Allele Identifier: CA2254836348
Gene: ANKRD13B HGNC NCBI
GIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29590679A= , CM000679.2:g.29590679A= GRCh38
NC_000017.10:g.27917697A= , CM000679.1:g.27917697A= GRCh37
NC_000017.9:g.24941823A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000487527.5:n.80+817A= (ANKRD13B)
ENST00000583413.4:c.88+3263T= (GIT1) ENSP00000466824.1:n.88+3263T=
ENST00000583728.5:c.-283+817A= (ANKRD13B) ENSP00000467078.1:n.-283+817A=
XM_017024174.2:c.-283+817A= (ANKRD13B) XP_016879663.1:n.-283+817A=