Canonical Allele Identifier: CA337456659
Gene: LINC00278 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.3004542G>C
GRCh37 chrY:g.2872583G>C
gnomAD v3:
Y:3004542 G / C
gnomAD v4:
chrY-3004542-G-C
Joint Max Group AF 0.00236049 (AFR)
Genomes Max Group AF 0.00236049 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3004542G>C , CM000686.2:g.3004542G>C GRCh38
NC_000024.9:g.2872583G>C , CM000686.1:g.2872583G>C GRCh37
NC_000024.8:g.2932583G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.222+1325G>C
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