Canonical Allele Identifier: CA821223608
Gene:

Linked Data

dbSNP Id: rs1224460546
MyVariant Identifiers: chr6:g.156133626T>A (hg19) chr6:g.155812492T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812492T>A , CM000668.2:g.155812492T>A GRCh38
NC_000006.11:g.156133626T>A , CM000668.1:g.156133626T>A GRCh37
NC_000006.10:g.156175318T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19073T>A
XR_943146.1:n.645-453A>T
XR_001744423.1:n.699-453A>T
XR_001744424.1:n.79+19073T>A
Search 100 bp 5'
Search 100 bp 3'