Canonical Allele Identifier: CA16042152
Gene: PALB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371919
dbSNP Id: rs1057517585

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23641155C>T , CM000678.2:g.23641155C>T GRCh38
NC_000016.8:g.23559977C>T NCBI36
NC_000016.9:g.23652476C>T , CM000678.1:g.23652476C>T GRCh37
NG_007406.1:g.5203G>A , LRG_308:g.5203G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261584.8:c.3G>A
ENST00000567003.1:n.147G>A
ENST00000568219.5:c.-866G>A ENSP00000454703.2:p.=
NM_024675.3:c.3G>A , LRG_308t1:c.3G>A
XM_011545948.1:c.-1017G>A XP_011544250.1:p.=