Canonical Allele Identifier: CA552614271

Gene: ALB

Linked Data

• dbSNP Id: rs1442960574
• gnomAD v2: 4-74274755-T-C
• gnomAD v3: 4-73409038-T-C
• gnomAD v4: 4-73409038-T-C
• COSMIC: COSN2044082
• MyVariant Identifiers: chr4:g.74274755T>C (hg19) ; chr4:g.73409038T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409038T>C , CM000666.2:g.73409038T>C	GRCh38
NC_000004.11:g.74274755T>C , CM000666.1:g.74274755T>C	GRCh37
NC_000004.10:g.74493619T>C	NCBI36
NG_009291.1:g.9784T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+233T>C MANE Select	ENSP00000295897.4:n.482+233T>C
ENST00000295897.8:c.482+233T>C	ENSP00000295897.4:n.482+233T>C
ENST00000401494.7:c.138-317T>C	ENSP00000384695.3:n.138-317T>C
ENST00000415165.6:c.138-2958T>C	ENSP00000401820.2:n.138-2958T>C
ENST00000441319.5:c.488+233T>C	ENSP00000392541.1:n.488+233T>C
ENST00000476441.6:c.80-317T>C	ENSP00000423727.1:n.80-317T>C
ENST00000503124.5:c.33-317T>C	ENSP00000421027.1:n.33-317T>C
ENST00000505649.5:n.168+233T>C
ENST00000509063.5:c.482+233T>C	ENSP00000422784.1:n.482+233T>C
ENST00000514786.1:n.451+233T>C
ENST00000621085.4:c.482+233T>C	ENSP00000483421.1:n.482+233T>C
ENST00000621628.4:c.483-35T>C	ENSP00000480485.1:n.483-35T>C
NM_000477.5:c.482+233T>C	NP_000468.1:n.482+233T>C
NM_000477.6:c.482+233T>C	NP_000468.1:n.482+233T>C
NM_000477.7:c.482+233T>C MANE Select	NP_000468.1:n.482+233T>C