Canonical Allele Identifier: CA823931727

Gene: TNXB ATF6B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32103240C>T , CM000668.2:g.32103240C>T	GRCh38
NC_000006.11:g.32071017C>T , CM000668.1:g.32071017C>T	GRCh37
NC_000006.10:g.32178995C>T	NCBI36
NG_008337.2:g.11135G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644971.2:c.-8-5034G>A (TNXB) MANE Select	ENSP00000496448.1:n.-8-5034G>A
ENST00000647633.1:c.-8-5034G>A (TNXB)	ENSP00000497649.1:n.-8-5034G>A
ENST00000375244.7:c.-8-5034G>A (TNXB)	ENSP00000364393.3:n.-8-5034G>A
ENST00000442721.1:c.-8-5034G>A (TNXB)	ENSP00000389946.1:n.-8-5034G>A
ENST00000479795.1:c.-8-5034G>A (TNXB)	ENSP00000418248.1:n.-8-5034G>A
ENST00000486148.1:n.42-5034G>A (TNXB)
ENST00000494022.1:n.290-5034G>A (ATF6B)
NM_019105.6:c.-8-5034G>A (TNXB)	NP_061978.6:n.-8-5034G>A
NM_001365276.1:c.-8-5034G>A (TNXB)	NP_001352205.1:n.-8-5034G>A
NM_019105.7:c.-8-5034G>A (TNXB)	NP_061978.6:n.-8-5034G>A
NM_001365276.2:c.-8-5034G>A (TNXB) MANE Select	NP_001352205.1:n.-8-5034G>A
NM_019105.8:c.-8-5034G>A (TNXB)	NP_061978.6:n.-8-5034G>A