Canonical Allele Identifier: CA982839919
Gene: ANKRD13B HGNC NCBI
GIT1 HGNC NCBI

Linked Data

dbSNP Id: rs2033774776

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29590688_29590689del , CM000679.2:g.29590688_29590689del GRCh38
NC_000017.10:g.27917706_27917707del , CM000679.1:g.27917706_27917707del GRCh37
NC_000017.9:g.24941832_24941833del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000487527.5:n.80+826_80+827del (ANKRD13B)
ENST00000583413.4:c.88+3256_88+3257del (GIT1) ENSP00000466824.1:n.88+3256_88+3257del
ENST00000583728.5:c.-283+826_-283+827del (ANKRD13B) ENSP00000467078.1:n.-283+826_-283+827del
XM_017024174.2:c.-283+826_-283+827del (ANKRD13B) XP_016879663.1:n.-283+826_-283+827del