Canonical Allele Identifier: CA948006265

Gene: MIP

Linked Data

• dbSNP Id: rs1868552015
• gnomAD v3: 12-56450345-G-A
• gnomAD v4: 12-56450345-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450345G>A , CM000674.2:g.56450345G>A	GRCh38
NC_000012.11:g.56844129G>A , CM000674.1:g.56844129G>A	GRCh37
NC_000012.10:g.55130396G>A	NCBI36
NG_021397.1:g.9307C>T
NG_021397.2:g.23822C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1351C>T	ENSP00000497190.1:n.*1351C>T
ENST00000652304.1:c.*935C>T MANE Select	ENSP00000498622.1:n.*935C>T
ENST00000257979.4:c.*935C>T	ENSP00000257979.4:n.*935C>T
NM_012064.3:c.*935C>T	NP_036196.1:n.*935C>T
XM_011538354.1:c.*935C>T	XP_011536656.1:n.*935C>T
NM_012064.4:c.*935C>T MANE Select	NP_036196.1:n.*935C>T
XM_017019306.1:c.*935C>T	XP_016874795.1:n.*935C>T