Canonical Allele Identifier: CA821223460
Gene:

Linked Data

dbSNP Id: rs1246161279
gnomAD v3: 6-155812253-C-T
gnomAD v4: 6-155812253-C-T
MyVariant Identifiers: chr6:g.156133387C>T (hg19) chr6:g.155812253C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812253C>T , CM000668.2:g.155812253C>T GRCh38
NC_000006.11:g.156133387C>T , CM000668.1:g.156133387C>T GRCh37
NC_000006.10:g.156175079C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18834C>T
XR_943146.1:n.645-214G>A
XR_001744423.1:n.699-214G>A
XR_001744424.1:n.79+18834C>T
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