Canonical Allele Identifier: CA141288889
Gene:

Linked Data

dbSNP Id: rs11968814
gnomAD v2: 6-71776971-G-A
gnomAD v3: 6-71067268-G-A
gnomAD v4: 6-71067268-G-A
MyVariant Identifiers: chr6:g.71776971G>A (hg19) chr6:g.71067268G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.71067268G>A , CM000668.2:g.71067268G>A GRCh38
NC_000006.11:g.71776971G>A , CM000668.1:g.71776971G>A GRCh37
NC_000006.10:g.71833692G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942677.1:n.36+7653G>A
Search 100 bp 5'
Search 100 bp 3'