Canonical Allele Identifier: CA440675886
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463769T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542612T>C , CM000666.2:g.105542612T>C GRCh38
NC_000004.11:g.106463769T>C , CM000666.1:g.106463769T>C GRCh37
NC_000004.10:g.106683218T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.393A>G
XR_939039.1:n.553A>G
XR_939040.1:n.296-1136A>G
XR_001741410.1:n.408A>G
XR_001741411.1:n.884A>G
XR_001741412.1:n.408A>G
XR_001741413.1:n.408A>G
XR_001741414.1:n.408A>G
XR_939038.2:n.408A>G
XR_939040.2:n.311-1136A>G