Canonical Allele Identifier: CA2254836359
Gene: ANKRD13B HGNC NCBI
GIT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29590710G= , CM000679.2:g.29590710G= GRCh38
NC_000017.10:g.27917728G= , CM000679.1:g.27917728G= GRCh37
NC_000017.9:g.24941854G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000487527.5:n.80+848G= (ANKRD13B)
ENST00000583413.4:c.88+3232C= (GIT1) ENSP00000466824.1:n.88+3232C=
ENST00000583728.5:c.-283+848G= (ANKRD13B) ENSP00000467078.1:n.-283+848G=
XM_017024174.2:c.-283+848G= (ANKRD13B) XP_016879663.1:n.-283+848G=
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