Canonical Allele Identifier: CA2404045754

Gene: PVALB

Linked Data

• dbSNP Id: rs1601523163

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36813219A>G , CM000684.2:g.36813219A>G	GRCh38
NC_000022.10:g.37209263A>G , CM000684.1:g.37209263A>G	GRCh37
NC_000022.9:g.35539209A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.304+427T>C MANE Select	ENSP00000400247.2:n.304+427T>C
ENST00000216200.9:c.304+427T>C	ENSP00000216200.5:n.304+427T>C
ENST00000404171.1:c.208+427T>C	ENSP00000386089.1:n.208+427T>C
ENST00000406910.6:c.300+427T>C
ENST00000417718.6:c.304+427T>C	ENSP00000400247.2:n.304+427T>C
NM_001315532.1:c.304+427T>C	NP_001302461.1:n.304+427T>C
NM_002854.2:c.304+427T>C	NP_002845.1:n.304+427T>C
XM_011530288.1:c.304+427T>C	XP_011528590.1:n.304+427T>C
NM_001315532.2:c.304+427T>C MANE Select	NP_001302461.1:n.304+427T>C
NM_002854.3:c.304+427T>C	NP_002845.1:n.304+427T>C