Canonical Allele Identifier: CA825142473
Gene:

Linked Data

dbSNP Id: rs1244397589
gnomAD v3: 6-465866-G-T
gnomAD v4: 6-465866-G-T
MyVariant Identifiers: chr6:g.465866G>T (hg19) chr6:g.465866G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465866G>T , CM000668.2:g.465866G>T GRCh38
NC_000006.11:g.465866G>T , CM000668.1:g.465866G>T GRCh37
NC_000006.10:g.410866G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12141G>T
XR_926365.1:n.2548+12141G>T
XR_001743914.1:n.482-9342G>T
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