Canonical Allele Identifier: CA1623760217
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1772001383
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751215_41751216insCAT , CM000668.2:g.41751215_41751216insCAT GRCh38
NC_000006.11:g.41718953_41718954insCAT , CM000668.1:g.41718953_41718954insCAT GRCh37
NC_000006.10:g.41826931_41826932insCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2682_71+2683insATG ENSP00000399429.1:n.71+2682_71+2683insATG
Search 100 bp 5'
Search 100 bp 3'