Canonical Allele Identifier: CA838978895
Gene:

Linked Data

dbSNP Id: rs1274112490
MyVariant Identifiers: chr7:g.46392572G>A (hg19) chr7:g.46352974G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352974G>A , CM000669.2:g.46352974G>A GRCh38
NC_000007.13:g.46392572G>A , CM000669.1:g.46392572G>A GRCh37
NC_000007.12:g.46359097G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3143G>A
XR_927242.1:n.3051G>A
XR_927241.2:n.3143G>A
XR_927242.2:n.3108G>A
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