Canonical Allele Identifier: CA12389876
Gene:
dbSNP:
4140535
gnomAD v2:
6:78175052 G / A
gnomAD v3:
6:77465335 G / A
gnomAD v4:
chr6-77465335-G-A
Joint Max Group AF 0.61308213 (EAS)
Genomes Max Group AF 0.61308213 (EAS)
MyVariant.info:
GRCh38 chr6:g.77465335G>A
GRCh37 chr6:g.78175052G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.77465335G>A , CM000668.2:g.77465335G>A GRCh38
NC_000006.11:g.78175052G>A , CM000668.1:g.78175052G>A GRCh37
NC_000006.10:g.78231771G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942706.1:n.545-9191G>A
XR_942707.1:n.545-9191G>A
XR_942708.1:n.545-9191G>A
XR_942709.1:n.545-9191G>A
XR_942708.2:n.545-9191G>A
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