Canonical Allele Identifier: CA148501658
Gene:

Linked Data

dbSNP Id: rs11760067
gnomAD v2: 6-135094272-C-T
gnomAD v3: 6-134773134-C-T
gnomAD v4: 6-134773134-C-T
MyVariant Identifiers: chr6:g.135094272C>T (hg19) chr6:g.134773134C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773134C>T , CM000668.2:g.134773134C>T GRCh38
NC_000006.11:g.135094272C>T , CM000668.1:g.135094272C>T GRCh37
NC_000006.10:g.135135965C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32604G>A
XR_943009.1:n.368+32604G>A
XR_001744363.1:n.414+32604G>A
XR_001744364.1:n.342+32604G>A
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