Canonical Allele Identifier: CA20854744
Gene: MTF1 HGNC NCBI

Linked Data

dbSNP Id: rs918348300
MyVariant Identifiers: chr1:g.38278791A>C (hg19) chr1:g.37813119A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.37813119A>C , CM000663.2:g.37813119A>C GRCh38
NC_000001.10:g.38278791A>C , CM000663.1:g.38278791A>C GRCh37
NC_000001.9:g.38051378A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373036.5:c.*2017T>G MANE Select ENSP00000362127.3:n.*2017T>G
ENST00000373036.4:c.*2017T>G ENSP00000362127.3:n.*2017T>G
NM_005955.2:c.*2017T>G NP_005946.2:n.*2017T>G
XM_011541491.1:c.*2017T>G XP_011539793.1:n.*2017T>G
XM_011541492.1:c.*2017T>G XP_011539794.1:n.*2017T>G
XM_011541494.1:c.*2017T>G XP_011539796.1:n.*2017T>G
XM_011541491.2:c.*2017T>G XP_011539793.1:n.*2017T>G
NM_005955.3:c.*2017T>G MANE Select NP_005946.2:n.*2017T>G
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