Canonical Allele Identifier: CA432619152
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216608T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175101T>G , CM000665.2:g.15175101T>G GRCh38
NC_000003.11:g.15216608T>G , CM000665.1:g.15216608T>G GRCh37
NC_000003.10:g.15191612T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000446690.2:n.1103A>C
ENST00000487147.5:n.927A>C
ENST00000491915.1:n.3A>C
NR_027927.1:n.1103A>C
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