Canonical Allele Identifier: CA440675943
Gene:

Linked Data

dbSNP Id: rs1323214595
MyVariant Identifiers: chr4:g.106463789G>A (hg19) chr4:g.105542632G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542632G>A , CM000666.2:g.105542632G>A GRCh38
NC_000004.11:g.106463789G>A , CM000666.1:g.106463789G>A GRCh37
NC_000004.10:g.106683238G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.373C>T
XR_939039.1:n.533C>T
XR_939040.1:n.296-1156C>T
XR_001741410.1:n.388C>T
XR_001741411.1:n.864C>T
XR_001741412.1:n.388C>T
XR_001741413.1:n.388C>T
XR_001741414.1:n.388C>T
XR_939038.2:n.388C>T
XR_939040.2:n.311-1156C>T
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