Canonical Allele Identifier: CA323997645

Gene: PVALB

Linked Data

• dbSNP Id: rs1036539461
• MyVariant Identifiers: chr22:g.37209498T>C (hg19) ; chr22:g.36813454T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36813454T>C , CM000684.2:g.36813454T>C	GRCh38
NC_000022.10:g.37209498T>C , CM000684.1:g.37209498T>C	GRCh37
NC_000022.9:g.35539444T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.304+192A>G MANE Select	ENSP00000400247.2:n.304+192A>G
ENST00000216200.9:c.304+192A>G	ENSP00000216200.5:n.304+192A>G
ENST00000404171.1:c.208+192A>G	ENSP00000386089.1:n.208+192A>G
ENST00000406910.6:c.300+192A>G
ENST00000417718.6:c.304+192A>G	ENSP00000400247.2:n.304+192A>G
ENST00000467935.1:n.526A>G
NM_001315532.1:c.304+192A>G	NP_001302461.1:n.304+192A>G
NM_002854.2:c.304+192A>G	NP_002845.1:n.304+192A>G
XM_011530288.1:c.304+192A>G	XP_011528590.1:n.304+192A>G
NM_001315532.2:c.304+192A>G MANE Select	NP_001302461.1:n.304+192A>G
NM_002854.3:c.304+192A>G	NP_002845.1:n.304+192A>G