Canonical Allele Identifier: CA2619338722
Gene: MIP HGNC NCBI

Linked Data

gnomAD v4: 12-56450303-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450303C>T , CM000674.2:g.56450303C>T GRCh38
NC_000012.11:g.56844087C>T , CM000674.1:g.56844087C>T GRCh37
NC_000012.10:g.55130354C>T NCBI36
NG_021397.1:g.9349G>A
NG_021397.2:g.23864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1393G>A ENSP00000497190.1:n.*1393G>A
ENST00000652304.1:c.*977G>A MANE Select ENSP00000498622.1:n.*977G>A
ENST00000257979.4:c.*977G>A ENSP00000257979.4:n.*977G>A
NM_012064.3:c.*977G>A NP_036196.1:n.*977G>A
XM_011538354.1:c.*977G>A XP_011536656.1:n.*977G>A
NM_012064.4:c.*977G>A MANE Select NP_036196.1:n.*977G>A
XM_017019306.1:c.*977G>A XP_016874795.1:n.*977G>A
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