Canonical Allele Identifier: CA1291598698

Gene: THSD7B

Linked Data

• dbSNP Id: rs1688061078

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.137469951G>C , CM000664.2:g.137469951G>C	GRCh38
NC_000002.11:g.138227521G>C , CM000664.1:g.138227521G>C	GRCh37
NC_000002.10:g.137943991G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409968.6:c.3138+18928G>C MANE Select	ENSP00000387145.1:n.3138+18928G>C
ENST00000272643.7:c.3139+18927G>C	ENSP00000272643.4:n.3139+18927G>C
ENST00000409968.5:c.3138+18928G>C	ENSP00000387145.1:n.3138+18928G>C
ENST00000413152.3:c.3046+18927G>C	ENSP00000413841.3:n.3046+18927G>C
NM_001080427.1:c.3045+18928G>C	NP_001073896.1:n.3045+18928G>C
NM_001316349.1:c.3138+18928G>C	NP_001303278.1:n.3138+18928G>C
XM_017005049.1:c.1341+18928G>C	XP_016860538.1:n.1341+18928G>C
NM_001316349.2:c.3138+18928G>C MANE Select	NP_001303278.1:n.3138+18928G>C