Canonical Allele Identifier: CA103381319
Gene:

Linked Data

dbSNP Id: rs1051758991
MyVariant Identifiers: chr4:g.106463943A>G (hg19) chr4:g.105542786A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542786A>G , CM000666.2:g.105542786A>G GRCh38
NC_000004.11:g.106463943A>G , CM000666.1:g.106463943A>G GRCh37
NC_000004.10:g.106683392A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-77T>C
XR_939039.1:n.456-77T>C
XR_939040.1:n.296-1310T>C
XR_001741410.1:n.311-77T>C
XR_001741411.1:n.787-77T>C
XR_001741412.1:n.311-77T>C
XR_001741413.1:n.311-77T>C
XR_001741414.1:n.311-77T>C
XR_939038.2:n.311-77T>C
XR_939040.2:n.311-1310T>C
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