Canonical Allele Identifier: CA1865199855
Gene: NUTM2F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94552459G>C , CM000671.2:g.94552459G>C GRCh38
NC_000009.11:g.97314741G>C , CM000671.1:g.97314741G>C GRCh37
NC_000009.10:g.96354562G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011518795.1:c.-3294+782C>G XP_011517097.1:n.-3294+782C>G
XM_011518796.1:c.-3294+782C>G XP_011517098.1:n.-3294+782C>G