Canonical Allele Identifier: CA824781317
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1208585833
MyVariant Identifiers: chr6:g.41718914T>C (hg19) chr6:g.41751176T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751176T>C , CM000668.2:g.41751176T>C GRCh38
NC_000006.11:g.41718914T>C , CM000668.1:g.41718914T>C GRCh37
NC_000006.10:g.41826892T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2722A>G ENSP00000399429.1:n.71+2722A>G
Search 100 bp 5'
Search 100 bp 3'