Canonical Allele Identifier: CA2404041484

Gene: PVALB

Linked Data

• dbSNP Id: rs1601518032

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36803639G>C , CM000684.2:g.36803639G>C	GRCh38
NC_000022.10:g.37199683G>C , CM000684.1:g.37199683G>C	GRCh37
NC_000022.9:g.35529629G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.305-2721C>G MANE Select	ENSP00000400247.2:n.305-2721C>G
ENST00000216200.9:c.305-2721C>G	ENSP00000216200.5:n.305-2721C>G
ENST00000404171.1:c.209-2721C>G	ENSP00000386089.1:n.209-2721C>G
ENST00000406910.6:c.351-2721C>G
ENST00000417718.6:c.305-2721C>G	ENSP00000400247.2:n.305-2721C>G
NM_001315532.1:c.305-2721C>G	NP_001302461.1:n.305-2721C>G
NM_002854.2:c.305-2721C>G	NP_002845.1:n.305-2721C>G
NM_001315532.2:c.305-2721C>G MANE Select	NP_001302461.1:n.305-2721C>G
NM_002854.3:c.305-2721C>G	NP_002845.1:n.305-2721C>G