Canonical Allele Identifier: CA1327521457
Community Standard Title: NC_000002.12:g.215766643C>G
Gene: LINC00607 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215766643C>G , CM000664.2:g.215766643C>G GRCh38
NC_000002.11:g.216631366C>G , CM000664.1:g.216631366C>G GRCh37
NC_000002.10:g.216339611C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_037195.1:n.212-16226G>C