Canonical Allele Identifier: CA736409255

Gene: TRABD2B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.47855549C>G , CM000663.2:g.47855549C>G	GRCh38
NC_000001.10:g.48321221C>G , CM000663.1:g.48321221C>G	GRCh37
NC_000001.9:g.48093808C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606738.3:c.667-53930G>C MANE Select	ENSP00000476820.1:n.667-53930G>C
ENST00000435576.2:n.180-53930G>C
ENST00000606738.2:c.667-53930G>C	ENSP00000476820.1:n.667-53930G>C
NM_001194986.1:c.667-53930G>C	NP_001181915.1:n.667-53930G>C
XM_006710640.2:c.667-53930G>C	XP_006710703.1:n.667-53930G>C
XM_011541442.1:c.667-53930G>C	XP_011539744.1:n.667-53930G>C
XM_011541443.1:c.667-53930G>C	XP_011539745.1:n.667-53930G>C
XM_011541444.1:c.667-53930G>C	XP_011539746.1:n.667-53930G>C
XM_011541445.1:c.667-53930G>C	XP_011539747.1:n.667-53930G>C
XR_426606.2:n.1247-53930G>C
XR_946653.1:n.1248-53930G>C
XR_946654.1:n.1248-53930G>C
XM_006710640.4:c.667-53930G>C	XP_006710703.1:n.667-53930G>C
XM_011541443.3:c.667-53930G>C	XP_011539745.1:n.667-53930G>C
XM_011541444.2:c.667-53930G>C	XP_011539746.1:n.667-53930G>C
XM_011541445.3:c.667-53930G>C	XP_011539747.1:n.667-53930G>C
XM_017001260.2:c.667-53930G>C	XP_016856749.1:n.667-53930G>C
XM_017001261.2:c.667-53930G>C	XP_016856750.1:n.667-53930G>C
XM_017001262.2:c.667-53930G>C	XP_016856751.1:n.667-53930G>C
XM_024446933.1:c.667-60789G>C	XP_024302701.1:n.667-60789G>C
XM_024446935.1:c.667-60789G>C	XP_024302703.1:n.667-60789G>C
XR_946654.3:n.1245-53930G>C
NM_001194986.2:c.667-53930G>C MANE Select	NP_001181915.1:n.667-53930G>C